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The Cochrane Database of Systematic Reviews logoLink to The Cochrane Database of Systematic Reviews
. 2004 Jan 26;2004(1):CD004668. doi: 10.1002/14651858.CD004668

Complex behavioural and educational interventions for nocturnal enuresis in children

Cathryn MA Glazener 1,, Jonathan HC Evans 2, Rachel E Peto 3
Editor: Cochrane Incontinence Group
PMCID: PMC12575883  PMID: 14974076

Abstract

Background

Nocturnal enuresis (bedwetting) is a socially disruptive and stressful condition which affects around 15 to 20% of five‐year olds, and up to 2% of young adults.

Objectives

To assess the effects of complex behavioural and educational interventions on nocturnal enuresis in children, and to compare them with other interventions.

Search methods

We searched the Cochrane Incontinence Group Specialised Trials Register (searched 20 March 2008) and the reference lists of relevant articles.

Selection criteria

All randomised or quasi‐randomised trials of complex behavioural or educational interventions for nocturnal enuresis in children were included, except those focused solely on daytime wetting. Comparison interventions included no treatment, simple and physical behavioural methods, alarms, desmopressin, tricyclic antidepressants, and miscellaneous other interventions.

Data collection and analysis

Two review authors independently assessed the quality of the eligible trials, and extracted data.

Main results

Eighteen trials involving 1174 children were identified which included a complex or educational intervention for nocturnal enuresis. The trials were mostly small and some had methodological problems including the use of a quasi‐randomised method of concealment of allocation in three trials and baseline differences between the groups in another three.

A complex intervention (such as dry bed training (DBT) or full spectrum home training (FSHT)) including an alarm was better than no‐treatment control groups (for example the relative risk (RR) for failure or relapse after stopping DBT was 0.25; 95% CI 0.16 to 0.39) but there was not enough evidence about the effects of complex interventions alone if an alarm was not used. A complex intervention on its own was not as good as an alarm on its own or the intervention supplemented by an alarm (e.g. RR for failure or relapse after DBT alone versus DBT plus alarm was 2.81; 95% CI 1.80 to 4.38). On the other hand, a complex intervention supplemented by a bed alarm might reduce the relapse rate compared with the alarm on its own (e.g. RR for failure or relapse after DBT plus alarm versus alarm alone was 0.5; 95% CI 0.31 to 0.80).

There was not enough evidence to judge whether providing educational information about enuresis was effective, irrespective of method of delivery. There was some evidence that direct contact between families and therapists enhanced the effect of a complex intervention, and that increased contact and support enhanced a package of simple behavioural interventions, but these were addressed only in single trials and the results would need to be confirmed by further randomised controlled trials, in particular the effect on use of resources.

Authors' conclusions

Although DBT and FSHT were better than no treatment when used in combination with an alarm, there was insufficient evidence to support their use without an alarm. An alarm on its own was also better than DBT on its own, but there was some evidence that combining an alarm with DBT was better than an alarm on its own, suggesting that DBT may augment the effect of an alarm. There was also some evidence that direct contact with a therapist might enhance the effects of an intervention.

Keywords: Child, Humans, Patient Education as Topic, Behavior Therapy, Behavior Therapy/methods, Enuresis, Enuresis/therapy, Exercise Therapy, Exercise Therapy/methods

Plain language summary

Complex behavioural and educational interventions for bedwetting (nocturnal enuresis) in children

Night‐time bedwetting is common in childhood, and can cause stigma, stress and inconvenience. Bed alarms are the treatments which currently appear to work best in the long term. Complex interventions such as dry bed training can also be tried. This involves, as well as using an alarm to wake the child after he or she has wet the bed, getting them to go to the toilet repeatedly and changing their own sheets. The review found 18 trials in 1174 children who had received this sort of training or another treatment. Although an alarm on its own was better than the dry bed training on its own, there was some evidence that using them together might reduce the relapse rate after stopping alarm treatment, and without the adverse effects of drug treatment. However, both using an alarm and dry bed training needs time and effort from the child and family. There was not enough research comparing complex interventions with other techniques.

Background

This is one of seven reviews of interventions for bedwetting, or non‐organic nocturnal enuresis. The others focus on: desmopressin (Glazener 2002), tricyclic antidepressants and related drugs (Glazener 2003a), other drugs (Glazener 2003b), simple behavioural training (Glazener 2004), alarms (Glazener 2005b) and complementary and miscellaneous other therapies (Glazener 2005a). All seven were originally based on the work of Lister‐Sharp and her colleagues at the Centre for Reviews and Dissemination at the University of York, UK (Lister‐Sharp 1997). The current review concerns the use of complex behavioural interventions (for example dry bed training (DBT) or full spectrum home training (FSHT)) or educational initiatives to train the child. It is restricted to children with monosymptomatic nocturnal enuresis who are treated with complex behavioural or educational interventions, and includes other interventions if they are compared with such methods or used in combination with them.

Description of the condition

Nocturnal enuresis is the involuntary loss of urine at night, in the absence of organic disease and at an age when a child could reasonably be expected to be dry (by consensus, at a developmental age of five years) (APA 1980; WHO 1992). Although bedwetting in itself is pathologically benign and has a high rate of spontaneous remission, it may bring social and emotional stigma, and stress and inconvenience to both the person with enuresis and their families (Fitzwater 1992). Children who wet the bed may experience parental disapproval, sibling teasing and repeated treatment failure which may all lower self esteem (Warzak 1992). The children may also be at increased risk of emotional and physical abuse (Warzak 1992). Consequently, it is important that enuresis is properly managed on 'humane grounds' (Moffatt 1994).

Although daytime wetting is a significant problem and is often associated with bedwetting, it is usually considered separately. It has been suggested that there are different aetiologies underlying the two conditions (Jarvelin 1989). If daytime symptoms are present, investigations to identify physical causes such as urinary tract dysfunction, congenital malformation and neurogenic disorders are usually necessary (Djurhuus 1992). An organic cause is more often found in children with daytime wetting; more structural abnormalities and functional disorders of the urinary tract were found in daytime wetters than controls (Jarvelin 1990).

Prevalences and causes

Nocturnal enuresis is a complaint that affects many families. Estimating the prevalence of nocturnal enuresis is difficult, however, due to the variation in methods of diagnosis and definitions used (de Jonge 1973; Krantz 1994). In the United Kingdom, the generally quoted prevalence rates are that 15% to 20% of five year olds, 7% of seven year olds, 5% of ten year olds, 2% to 3% of 12 to 14 year olds and 1% to 2% of those aged 15 and over wet the bed on average twice a week (Blackwell 1989; Rutter 1973). Historically, the incidence of nocturnal enuresis was particularly high amongst children in residential care (Morgan 1970). About 1% of adults remain enuretic. Without treatment, about 15% of bedwetting children become dry each year (Forsythe 1974). However, it is not possible to predict which children will become dry spontaneously (Doleys 1977a).

The causes of nocturnal enuresis are unclear (Lister‐Sharp 1997). Genetic (APA 1980; Bakwin 1971; Bakwin 1973; Eiberg 1995), physiological (Djurhuus 1992; Norgaard 1993) and psychological (Devlin 1991; Moffatt 1989; Rutter 1973; Shaffer 1977) factors, as well as delay in maturation of the mechanism for bladder control (Jarvelin 1989; Koff 1995), have been suggested. Other factors which may contribute to bedwetting include: constipation, sleep apnoea and upper airway obstructive symptoms (Maizels 1993); and diet and mild caffeine drinks with diuretic effects (for example cola) (Blackwell 1989).

Interventions

Pharmacological, behavioural and a variety of other interventions are commonly used for people who wet the bed.

Pharmacological interventions include desmopressin, tricyclic drugs (amitriptyline, dothiepin, doxepin, trimipramine, clomipramine, desipramine, imipramine, lofepramine, nortriptyline and protriptyline), drugs related to the tricyclics (viloxazine, mianserin and maprotiline), and a variety of other drugs (for example amphetamine, diazepam and oxybutynin).

Behavioural interventions include simple interventions such as lifting, waking, reward systems, alarms, overlearning, retention control training and stop‐start training, and complex behavioural interventions such as dry‐bed training (DBT) and full spectrum home training (FSHT).

Educational interventions include different methods of providing information for children and their parents, or different methods of teaching or explanation for any other enuresis intervention.

Other and complementary interventions include counselling, psychotherapy, surgery and complementary therapies.

The current review was restricted to complex behavioural interventions, defined as those which use a number of different behavioural interventions in combination, and educational interventions. Other interventions were included if they were compared with such programmes.

Description of the intervention

Complex behavioural treatment programmes

Complex behavioural interventions include dry‐bed training and full spectrum home training.

Dry‐bed training (DBT)

Dry bed training was initially developed in the early 1970s for use with adults with learning disabilities (Azrin 1973). The original schedule involved an intensive training night, during which the patient was woken every hour and taken to the toilet. If an accident occurred, reprimands consisting of 45 minutes of 'cleanliness training' (changing the bed) and 'positive practice' (patient practices getting up and going to the toilet about nine times) were implemented. On subsequent nights, the individual was woken once and taken to the toilet, this nightly 'waking' occurring progressively earlier. Because of inherent difficulties in implementing this regimen, it has been modified. Variants such as Modified DBT forgo the reprimands and positive practice elements (Butler 1988). DBT may or may not include the use of an alarm to supplement the other elements of the programme.

Full spectrum home training (FSHT)

Full spectrum home training (Houts 1983; Howe 1992) combines a urine alarm triggered by wetting with cleanliness training, retention control training (teaching the children to retain progressively larger volumes of urine in their bladders during the day in order to try to increase bladder capacity) and over‐learning. For this, after successful alarm treatment, the children are given extra drinks at bed‐time to cause additional stress to the detrusor muscles in the bladder. Alarm treatment is then continued until 14 consecutive dry nights are once again achieved (Blackwell 1989).

Educational interventions

Educational interventions may range from those providing background information to parents or children about enuresis to specific materials prepared to advise users about how to implement various treatments (such as alarms or DBT). Some trials have compared different methods of delivery, such as oral, written, computer‐based (CD‐ROM) or using a video presentation, or different settings for teaching, such as home or clinic based.

Other interventions which were included in this review as comparisons were as follows:

Enuresis alarms

Enuresis alarms consist of some kind of alarm which is activated by inappropriate micturition. The first enuresis alarms were bed‐based, the child sleeping on a pad or mat containing an electrical circuit. When urine wets the pad, it completes the circuit causing a bell to ring. The alarm is intended to change the meaning of the sensation of having a full bladder from a signal to urinate to a signal to inhibit urination and waken (Forsythe 1989). There are now many variations: the alarm may be a bell, buzzer, visual signal such as a light or may vibrate. There are also many different tones and intensities. In 'mini‐alarm' systems, the sensor is placed in the pants, producing a discrete, portable system. Overlearning may be used to supplement successful alarm treatment.

Overlearning

An over‐learning procedure may be initiated after successful alarm treatment (for example achievement of 14 consecutive dry nights). Extra drinks are given at bed‐time to cause additional stress to the detrusor muscles in the bladder. Alarm treatment is then continued until 14 consecutive dry nights are again achieved (Blackwell 1989).

Simple behavioural interventions

Psychological interventions assume that the ability to remain dry at night is a learned response which can be achieved using conditioning techniques if it has not arisen spontaneously. These interventions include lifting, wakening, fluid restriction and reward systems.

Lifting

Carers 'lift' the child, while still asleep, out of bed to allow them to urinate in an appropriate place. It has been argued that this practice is counterproductive for a number of reasons. These include the child being denied the opportunity to learn the sensations that a full bladder produces and the child being encouraged to urinate without waking (Butler 1994). On the other hand, some suggest that lifting is effective, precluding the need for professional help (Shaffer 1977).

Scheduled wakening

This intervention involves waking the child to allow them to get up and urinate (Warzak 1994). A scheduled waking programme may be used with the child being woken progressively earlier after dry nights until the interval between going to bed and scheduled waking is one hour. Older individuals may use an alarm clock to wake themselves (Blackwell 1989).

Fluid restriction

This is a measure frequently implemented by parents (Shaffer 1977). Children are discouraged from drinking fluids in the evening before going to bed. However, fluid restriction may aggravate a low functional bladder capacity (Sorotzkin 1984). Even so, it might be useful to restrict drinks with diuretic properties (for example those containing caffeine such as cola), before retiring (Novello 1987).

Reward systems

Reward systems (for example star charts) are behavioural interventions which use positive reinforcement to encourage a desired behaviour. The child is rewarded for attaining an achievable goal, such as remaining dry all night ‐ or if this is too ambitious, an intermediate goal such as getting up to go to the toilet. These schemes should be negotiated with the child and family. The positive reinforcement of dry nights can help to reduce the negative emphasis on wet beds. These are often the first type of treatments proposed (Stewart 1975). However, unless used with care, a child may feel a failure if the reward is not attained (Blackwell 1989).

Retention control training and stop‐start training

Retention control training is an attempt to increase the functional bladder capacity using exercises such as delaying urination for extended periods of time or drinking increased fluids, analogous to bladder training in adults (Warzak 1994). The rationale is that if the bladder can hold larger volumes of urine, it will not empty so soon at night. In a review of simple behavioural interventions, retention control training was compared with no‐treatment controls, desmopressin and an alarm (Glazener 2004). There was not enough reliable evidence for any of the comparisons apart from with alarms, which were more effective than retention control training in one small trial (Bennett 1985). Stream interruption exercises may also be recommended, also called stop‐start training, and analogous to pelvic floor muscle training in adults (Novello 1987). The rationale is that strengthening the pelvic floor will help the child to control their wetting at night. However, no trials of stop‐start training alone were identified in the review (Glazener 2004).

Why it is important to do this review

The wide variety of treatments for nocturnal enuresis indicates the lack of consensus as to which is the best. Provided that a sufficient number of trials of adequate quality have been conducted, the most reliable evidence is likely to come from consideration of all well‐designed randomised controlled trials. Hence, there is a need for an easily accessible, periodically updated, comprehensive systematic review of such studies, which will not only help to identify optimal practice, but also highlight gaps in the evidence base.

Objectives

To determine the effects of complex behavioural or educational interventions for the treatment of children with nocturnal enuresis.

The following interventions were tested: 
 1. a complex behavioural intervention versus no active (control) treatment; 
 2. one complex behavioural intervention alone versus another behavioural intervention; 
 3. a complex behavioural intervention in combination with another behavioural intervention versus a behavioural intervention alone; 
 4. one method of delivery of training for a complex behavioural intervention versus another one; 
 5. one component of a complex behavioural intervention or combination of components versus another; 
 6. a complex intervention versus drug therapy; 
 7. an educational intervention versus no treatment; 
 8. one educational intervention versus another.

Methods

Criteria for considering studies for this review

Types of studies

Randomised or quasi‐randomised trials of complex behavioural or educational interventions for the treatment of non‐organic nocturnal enuresis.

Types of participants

Children (as defined by the trialists, usually up to age 16) suffering from nocturnal enuresis. Trials which included children suffering from daytime enuresis or where some children may have had an organic cause contributing to their enuresis were only included if the primary problem was nocturnal enuresis.

Types of interventions

Complex behavioural interventions such as dry‐bed training (DBT) or full spectrum home training (FSHT), and educational interventions such as providing information or teaching about enuresis or its management (for example how to implement a complex intervention). 
 Comparisons included no active treatment, with and without alarms, stop‐start training (pelvic floor muscle training and bladder training), retention control training, reward systems and wakening.

Types of outcome measures

The outcomes considered in this review were:

  • change in the mean number of wet nights per week during treatment;

  • number of participants failing to attain 14 consecutive dry nights;

  • mean number of wet nights per week when participants were followed up after treatment had ceased;

  • number failing to attain 14 consecutive dry nights or subsequently relapsing; and

  • adverse events.

Timing of relapse and follow up were as defined by the trialists.

Search methods for identification of studies

This review has drawn on the search strategy developed for the Incontinence Review Group. Relevant trials were identified from the Cochrane Incontinence Group Specialised Register of controlled trials which is described under the Incontinence Group's details in The Cochrane Library (Please see the ‘Specialized Register’ section of the Group’s module in The Cochrane Library.). The register contains trials identified from the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, CINAHL and hand searching of journals and conference proceedings. The date of the most recent search of the register for this review: 20 March 2008.

The trials in the Cochrane Incontinence Group Specialised Register are also contained in CENTRAL.

The terms used to search the Cochrane Incontinence Group Trial Register are given below: 
 (TOPIC.URINE.ENURESIS*) 
 AND 
 ({DESIGN.CCT*} OR {DESIGN.RCT*}) 
 (All searches were of the keyword field of Reference Manager 9.5 N, ISI ResearchSoft).

The reviewer authors also searched the reference lists of relevant articles. We did not impose any language or other restrictions on any of these searches.

Data collection and analysis

The studies for this review were assessed using the methods of The Cochrane Collaboration (Deeks 2005).

Selection of studies

The titles and, where possible, abstracts of all studies located by the searches were checked by two reviewer authors to identify those likely to be evaluations of the effects of interventions for nocturnal enuresis. Full papers were then obtained and assessed by two reviewer authors to identify those which met the inclusion criteria.

Data extraction and management

The data were extracted independently by two reviewer authors using a standard form. Differences were resolved by discussion.

Assessment of risk of bias in included studies

Each study was assessed using both general and specific quality criteria. The criteria applied were:

  • the level of concealment of random allocation in the trials (A = adequate method of concealment of allocation to groups, B = unclear, C = quasi‐randomised);

  • whether data to assess the comparability of groups at baseline were given, including baseline levels of wetting;

  • use of a 'wash‐out' period if a crossover design was employed;

  • intention‐to‐treat analysis;

  • whether outcomes were clearly defined;

  • blinding;

  • a follow up of at least three months or provision of follow‐up data;

  • whether useful data (for example means and standard deviations) were presented;

  • whether children with daytime wetting were specifically excluded;

  • whether children who had physical (organic) causes for their enuresis were specifically excluded.

However, none of these criteria were used to include or exclude trials.

Measures of treatment effect

Where appropriate, the results were converted to the mean and standard deviation of the number of wet nights per week; or the number of children failing to achieve cure during treatment, defined as 14 consecutive dry nights; or the number who were not cured during treatment plus those who relapsed after stopping active treatment (to allow for possible differences in initial 'success' rates). Where a mean value was reported with no standard deviation, we entered the data into 'Other data tables'.

Dealing with missing data

In general, dropouts were not taken into account and data were presented as given in the trial reports. However, if there was evidence of differential dropout from the groups which may have been caused by lack of response or adverse effects of the interventions, the data were recalculated as if the dropouts were failures.

Assessment of heterogeneity

Differences between trials were further investigated when statistically significant heterogeneity was found at the 10% probability level using the chi‐squared test or assessment of the I‐squared statistic (Higgins 2003), or appeared obvious from visual inspection of the results. If there was no obvious reason for the heterogeneity, or it persisted despite the removal of outlying trials, a random‐effects model could have been used. However, in the event this was not necessary.

Data synthesis

We intended, where possible, to calculate standardised effect sizes and 95% confidence intervals (CI); weighted mean differences (WMD) where outcomes were continuous variables and relative risks (RR) where they were binary. A fixed‐effect model was used to calculate the pooled estimates and the 95% CIs (Berlin 1989). The weighted mean differences were weighted by the inverse of the variance, and given as differences in number of wet nights per week. Negative values indicate fewer wet nights in the intervention group, at the left‐hand side of the tables.

Results

Description of studies

Results of the search

Of the studies identified for this review, 12 studies were excluded, and 18 trials were included. One study reference contained data from two trials (Houts 1987a; Houts 1987b).

Included studies

Size of trials

In the 18 included trials, a total of 1174 children were enrolled (an average of 65 per trial), of whom 746 received a complex behavioural or educational intervention. Total trial size ranged from 14 to 270 children. Further details are available in the Table Characteristics of included studies.

Interventions and comparisons

The complex or educational interventions identified comprised:

The comparison interventions included no‐treatment or waiting list controls, alarms, stop‐start training (sphincter muscle exercises and bladder training), imipramine, desmopressin, pelvic floor muscle training and motivational therapy or counselling.

Ages of the children

The majority of the trials recruited children between the ages of 5 and 16 years, but none subdivided their results between younger children and teenagers. On average, the mean age was 8 to 10 years. Three trials included a few children younger than five years old (Azrin 1974; Azrin 1978; Keating 1983).

Settings and populations

Three trials recruited children from the community (Azrin 1974; Nawaz 2002; Redsell 2003); in three trials, children came from both community advertisements and referrals (Houts 1986; Houts 1987a; Houts 1987b); and the remaining trials did not give details but were mostly submitted from hospital clinics. None of the trials included children with special needs or from residential settings.

Previous treatment

In six trials, some of the children had failed with previous treatment (Bollard 1981; Bollard 1982a; Bollard 1982b; Butler 1988; Nawaz 2002; Redsell 2003); in two all had previously failed (Butler 1990; Caceres 1982); in another three, none had received previous treatment (Bennett 1985; Fera 2004; Iester 1991); and in the remainder this was not mentioned. However, if the children had been treated before, this was stopped during or before they entered the trial.

Duration of treatment

In six trials, treatment was continued for eight weeks or less (Azrin 1974; Azrin 1978; Bollard 1982b; Caceres 1982; Fera 2004; Keating 1983). In the remainder, children continued for 10 to 20 weeks, or until achieving 14 dry nights.

Excluded studies

Of the studies identified for this review, 12 were excluded, most often because they were not randomised controlled trials. In five cases, randomised controlled trials were excluded because they included mainly adults (Azrin 1973; Hanson 1988); all the children had daytime wetting (Smith 1979); because protocol violations resulted in children being moved from their assigned groups and, therefore, the data became unreliable (not intention‐to‐treat, Doleys 1977b); or because data from different RCTs were combined and control data not given (Whelan 1990). Details are given in the Table Characteristics of excluded studies.

Risk of bias in included studies

Allocation

Only one trial (Redsell 2003) used an adequate method of randomisation with secure concealment of allocation, but despite this there were some baseline differences between the groups. Three trials used an inadequate method of concealment of allocation (quasi‐randomisation) (Azrin 1974; Butler 1988; Butler 1990) and the remainder did not give enough detail for this to be assessed.

In three trials, the children were found to be not comparable at baseline on some or all factors (Bollard 1982b; Houts 1987a; Redsell 2003); and in another four they were found to be comparable (Fera 2004; Houts 1986; Keating 1983; Nawaz 2002). The remainder did not provide this information.

Incomplete outcome data

In three trials (Bollard 1981; Bollard 1982b; Keating 1983) continuous data were presented without measures of dispersion (SDs), and in the latter two, means had to be estimated from graphs. In one trial no data were useable in a meta‐analysis due to amalgamation of data from groups (Azrin 1974). In another (van Kampen 2005) no useable data were presented, nor were numbers of children per group given.

In seven of the trials, data were presented after treatment stopped (Bennett 1985; Bollard 1981; Houts 1986; Houts 1987a; Iester 1991; Keating 1983; Redsell 2003).

In six trials, a few children dropped out from each group (Bennett 1985; Bollard 1981; Butler 1990; Houts 1986; Keating 1983; van Kampen 2005). The remainder either reported that there were no dropouts or presented data for all included children. However, in one trial, 12 out of 20 children dropped out from one group only, DBT without an alarm (Bollard 1981). These were counted as failed in meta‐analyses as the trialists stated that these children dropped out because they had a poor response. In another trial, children were much less likely to comply with treatment if they were randomised to imipramine or three‐step therapy (compared with three‐step therapy supplemented by counselling and education), although follow up data were provided for all children (Iester 1991).

Other potential sources of bias

Daytime wetting, organic causes and baseline recording of wetting

Children with organic causes were specifically excluded in 12 trials. Organic causes were either not mentioned or not excluded in seven trials (Bennett 1985; Bollard 1981; Caceres 1982; Fera 2004; Houts 1986; Houts 1987a; Houts 1987b). In seven trials, children with daytime wetting were definitely excluded (Azrin 1978; Butler 1990; Fera 2004; Houts 1987a; Houts 1987b; Keating 1983; Nawaz 2002). In one, some children with daytime wetting were included, although if they had an organic cause identified they were excluded (Bollard 1981); and in another they were only included if the daytime wetting was not significant (Bennett 1985). In one trial, some of the children did have daytime wetting, organic causes or behaviour problems (Caceres 1982). The remainder did not mention daytime wetting. Only one of the trials failed to give systematic details about baseline wetting before starting the trial (Iester 1991).

Effects of interventions

1. Complex or educational interventions versus no‐treatment controls (Analysis 1, Other data tables 1.2)

No‐treatment controls were compared with a variety of complex interventions:

If children were allocated to DBT or FSHT including an alarm triggered by wetting as part of the package, they had fewer wet nights (Analysis 1.1; Analysis 1.2) (Bennett 1985; Bollard 1982b; Nawaz 2002) and were more likely to become dry during treatment (e.g. RR for failure 0.17; 95% CI 0.11 to 0.28, Analysis 1.3.4) (Bollard 1981, Bollard 1982b; Bennett 1985; Nawaz 2002) and afterwards (e.g. RR for failure or relapse after stopping treatment 0.25; 95% CI 0.16 to 0.39, Analysis 1.4.4) (data from Groups A, B and C combined) (Bollard 1981) than those allocated to no‐treatment control groups. Although there appeared to be significant statistical heterogeneity between the trials (Analysis 1.3.4), this is likely to be a statistical artefact as it disappeared when the data were expressed as cure rather than failure rates.

1.1. Analysis.

1.1

Comparison 1 Complex interventions versus no‐treatment controls, Outcome 1 Mean number of wet nights per week on treatment.

1.2. Analysis.

Comparison 1 Complex interventions versus no‐treatment controls, Outcome 2 Mean number of wet nights per week on treatment (no SDs).

Mean number of wet nights per week on treatment (no SDs)
Study Complex Control
DBT (office training of parent and child, no alarm) vs control
Keating 1983 Mean 2.7 wet nights (n=7) Mean 2 wet nights (n=7)
DBT (home training of parent and child, no alarm) vs control
Keating 1983 Mean 2.5 wet nights (n=9) Mean 2 wet nights (n=7)
DBT (office training of parent only, no alarm) vs control
Keating 1983 Mean 1.9 wet nights (n=7) Mean 2 wet nights (n=7)
DBT with alarm vs control
Bollard 1981 Mean 0 wet nights (n=60) 
 (groups A, B and C) Mean 4.4 wet nights (n=20) 
 (group F)
Bollard 1982b Mean 0.2 wet nights (n=10) Mean 5.3 wet nights (n=10)
DBT without alarm vs control
Bollard 1981 Mean 3.8 wet nights (n=20) 
 (group D including dropouts) Mean 4.4 wet nights (n=20) 
 (group F)
Bollard 1982b Mean 3.25 wet nights (n=10) Mean 5.3 wet nights (n=10)
1.3. Analysis.

1.3

Comparison 1 Complex interventions versus no‐treatment controls, Outcome 3 Number not achieving 14 consecutive dry nights.

1.4. Analysis.

1.4

Comparison 1 Complex interventions versus no‐treatment controls, Outcome 4 Number failing or relapsing.

However, if the active arm did not include an alarm there was insufficient evidence to show a difference (e.g. RR for failure 0.82; 95% CI 0.66 to 1.02, Analysis 1.3.6) (Bollard 1981; Bollard 1982b; Redsell 2003). The same pattern emerged when relapse after stopping treatment was taken into account (Analysis 1.4.6). However, most of the trials were small, and most comparisons were addressed only by single trials.

2. Complex interventions alone versus other behavioural interventions (Analysis 2, Other data tables 2.2)

Two main types of complex intervention alone (without an alarm) were included:

These complex interventions were compared with:

Judged both on number of wet nights and failure rates during treatment, and combined failure and relapse rates after treatment finished, a complex intervention on its own was not as good as:

  • an alarm (e.g. RR for failure or relapse 1.7; 95% CI 1.06 to 2.73, Analysis 2.3.1) (Bollard 1981) ;

  • DBT plus an alarm (e.g. RR for failure or relapse 2.81; 95% CI 1.80 to 4.38, Analysis 2.3.2) (Bollard 1981; Bollard 1982b) ; or

  • a three‐step programme (retention control training, wakening and parental reassurance) supplemented by counselling and educational reinforcement (e.g. RR for failure or relapse 2.07; 95% CI 1.16 to 3.72, Analysis 2.3.3) (Iester 1991) .

2.3. Analysis.

2.3

Comparison 2 Complex interventions alone versus other behavioural interventions, Outcome 3 Number failing or relapsing.

3. Supplemented complex interventions versus other behavioural interventions (Analyses 3 and 4, Other data tables 3.2)

Two main types of complex interventions supplemented by other behavioural interventions were included:

These complex interventions were compared with:

Although there was no consistent pattern of difference between supplemented complex interventions and their comparison interventions, the trials were mostly small or individual comparisons were addressed only by single trials. There was significant heterogeneity (P value 0.01, I‐squared 76.7%) for the only comparison reported in more than one trial (DBT plus alarm versus alarm alone, Analysis 3.3.03). This could have been due to the inclusion of one trial (Butler 1990) which used different types of alarms in the two arms (bed alarm plus DBT in one versus pants alarm in the other). All the included children in this trial had already failed using a standard bed alarm. Exclusion of this trial reduced or removed the heterogeneity (sensitivity analysis, Analysis 4.1; Analysis 4.2). Thus, the data marginally favoured supplementing DBT with an alarm: compared with an alarm only, the RR for failure during treatment was 0.6; 95% CI 0.38 to 0.94, (Analysis 4.1) in four trials (Bennett 1985; Bollard 1981; Butler 1988; Nawaz 2002); and the RR for failure or relapse was 0.50; 95% CI 0.31 to 0.80 (Analysis 4.2) in two trials (Bollard 1981; Nawaz 2002): (data from Groups A, B and C combined in one trial, Bollard 1981).

3.3. Analysis.

3.3

Comparison 3 Supplemented complex interventions versus other behavioural interventions, Outcome 3 Number not achieving 14 consecutive dry nights.

4.1. Analysis.

4.1

Comparison 4 Sensitivity analysis: supplemented complex interventions versus other behavioural interventions, Outcome 1 Number not achieving 14 consecutive dry nights.

4.2. Analysis.

4.2

Comparison 4 Sensitivity analysis: supplemented complex interventions versus other behavioural interventions, Outcome 2 Number failing or relapsing.

5. Complex interventions ‐ different training regimens (Analysis 5, Other data tables 5.1)

Four trials addressed the issue of different methods of providing instruction to children or parents regarding the implementation of complex behavioural interventions (Bollard 1981; Houts 1987a; Houts 1987b; Keating 1983).

The trials were small or addressed only single interventions. There was not enough evidence to suggest that any method was better than another, except that live delivery of FSHT was better than filmed delivery in two small trials (RR for failure during treatment 0.36; 95% CI 0.15 to 0.90, Analysis 5.2.7) (Houts 1987a; Houts 1987b), suggesting that interaction with a person may have a positive supportive effect.

5.2. Analysis.

5.2

Comparison 5 Complex interventions ‐ different training regimens, Outcome 2 Number not achieving 14 consecutive dry nights.

6. Comparing components of complex interventions (Analysis 6, Other data tables 6.1)

In one trial (Bollard 1982a), trialists tried to unpick the various components of the dry bed training regimen to identify if one component or combination of components was more effective than any other component. However, the number of children in each of the arms was too small to allow meaningful conclusions to be drawn (Analysis 6.1, Analysis 6.2).

6.1. Analysis.

Comparison 6 Comparing components of complex interventions, Outcome 1 Mean number of wet nights per week on treatment (no SDs).

Mean number of wet nights per week on treatment (no SDs)
Study Component X Component Y
alarm + waking VS alarm + retention control training
Bollard 1982a Mean 1.35 wet nights (n=12) Mean 1.2 wet nights (n=12)
alarm + waking VS alarm + positive practice+ cleanliness training
Bollard 1982a Mean 1.35 wet nights (n=12) Mean 1.15 wet nights (n=12)
alarm + waking VS alarm + waking + retention control training
Bollard 1982a Mean 1.35 wet nights (n=12) Mean 0.7 wet nights (n=12)
alarm + waking VS alarm + waking + positive practice + cleanliness training
Bollard 1982a Mean 1.35 wet nights (n=12) Mean 0.5 wet nights (n=12)
alarm + waking VS alarm + retention control training + positive practice + cleanliness training
Bollard 1982a Mean 1.35 wet nights (n=12) Mean 1.05 wet nights (n=12)
alarm + retention control training VS alarm + positive practice+ cleanliness training
Bollard 1982a Mean 1.2 wet nights (n=12) Mean 1.15 wet nights (n=12)
alarm + retention control training VS alarm + waking + retention control training
Bollard 1982a Mean 1.2 wet nights (n=12) Mean 0.7 wet nights (n=12)
alarm + retention control training VS alarm + waking + positive practice + cleanliness training
Bollard 1982a Mean 1.2 wet nights (n=12) Mean 0.5 wet nights (n=12)
alarm + retention control training VS alarm + retention control training + positive practice + CT
Bollard 1982a Mean 1.2 wet nights (n=12) Mean 1.05 wet nights (n=12)
alarm + positive practice + cleanliness VS alarm + waking + retention control training
Bollard 1982a Mean 1.15 wet nights (n=12) Mean 0.7 wet nights (n=12)
alarm + positive practice + cleanliness VS alarm + waking + positive practice + cleanliness training
Bollard 1982a Mean 1.15 wet nights (n=12) Mean 0.5 wet nights (n=12)
alarm + positive practice + cleanliness training VS alarm + retention control training + PP + CT
Bollard 1982a Mean 1.15 wet nights (n=12) Mean 1.05 wet nights (n=12)
alarm + waking + retention control training VS alarm + waking + positive practice + cleanliness training
Bollard 1982a Mean 0.7 wet nights (n=12) Mean 0.5 wet nights (n=12)
alarm + waking + retention control training VS alarm + retention control training + positive practice + CT
Bollard 1982a Mean 0.7 wet nights (n=12) Mean 1.05 wet nights (n=12)
alarm + waking + positive practice + cleanliness training VS alarm + retention control training + PP + CT
Bollard 1982a Mean 0.5 wet nights (n=12) Mean 1.05 wet nights (n=12)
6.2. Analysis.

6.2

Comparison 6 Comparing components of complex interventions, Outcome 2 Number not achieving 14 dry nights.

7. Complex interventions versus drugs (Analysis 7)

In one trial (Iester 1991), a three‐step regimen (retention control training, wakening and parental reassurance) with and without supplemental counselling and educational reinforcement seemed to be better than imipramine alone (for example when supplemented, RR for failure and relapse 0.27; 95% CI 0.16 to 0.43, Analysis 7.3.2).

7.3. Analysis.

7.3

Comparison 7 Complex interventions versus drugs, Outcome 3 Number failing or relapsing.

In another trial (Fera 2004), children receiving an assortment of behaviour modification methods (dietary and fluid adjustment, voiding schedules, double voiding, bedtime toileting, alarm clock once at night, pelvic floor training, environmental modifications, changes in parents' attitudes, improvement of self‐esteem, self care) had more wet nights than those receiving desmopressin (WMD 1.67, 95% CI 0.35 to 2.99, Analysis 7.2) (Fera 2004) but the numbers were too few to assess failure rates and there were no follow up data.

7.2. Analysis.

7.2

Comparison 7 Complex interventions versus drugs, Outcome 2 Mean number of wet nights per week on treatment.

8. Educational interventions versus no‐treatment controls (Analysis 8)

No‐treatment controls were compared with two different methods of educating children and their parents about enuresis: interactive CD‐ROM or leaflets (Redsell 2003). Although there appeared to be no effect of the educational information on outcome (e.g. RR for failure or relapse 1.06, 95% CI 0.91 to 1.24, Analysis 8.2.1), the groups were small and the confidence intervals wide.

8.2. Analysis.

8.2

Comparison 8 Educational interventions versus no‐treatment controls, Outcome 2 Number failing or relapsing.

9. Educational interventions compared (Analysis 9)

One trial compared two methods of method of delivery of information (interactive CD‐ROM versus leaflets) about enuresis (Redsell 2003). Again, there was no apparent effect on outcome (e.g. RR for failure or relapse 1.15, 95% CI 0.97 to 1.36, Analysis 9.2) but the single trial was small.

9.2. Analysis.

9.2

Comparison 9 Different educational interventions compared, Outcome 2 Number failing or relapsing.

Adverse effects

None of the trialists mentioned whether or not there were any adverse effects. However, in one trial, the interventions were found to be impractical (DBT, two families refused to implement it) or disruptive (another family could not use the alarm for fear of waking a neighbour) (Caceres 1982).

Costs

None of the trials gave information about the relative costs of the interventions.

Discussion

Summary of main results

Despite the methodological shortcomings of some of the trials, DBT or FSHT including an alarm were better than no‐treatment controls, but the evidence supporting their use without an alarm was inconclusive. However, when the DBT or FSHT on their own were compared with an alarm on its own (or an alarm plus DBT), the alarm arm was clearly better than the complex method without an alarm, suggesting that it was the alarm rather than the DBT which was important. A different programme which combined three simple interventions was improved when supplemented by counselling and educational reinforcement, suggesting that extra input from therapists might enhance effectiveness. The compliance rate was highest in the group which had the most contact.

A combination of DBT plus alarm might be better than an alarm on its own, suggesting that DBT may have an additive effect although the data came from only two small trials. Trials involving FSHT, or comparisons with retention control training or stop‐start training were too small to provide reliable data.

Trials which addressed different methods of delivery of the interventions or the effectiveness of providing information about enuresis were mostly too small to provide reliable information. However, one comparison of a therapist delivering instructions 'live' to a group of parents and children (compared with imparting the same information by videotape) showed that the live delivery had better results, at least initially (Houts 1987a; Houts 1987b). As both groups demonstrated equal gains in information, the difference was attributed to psychological support from the direct contact with the therapist.

Although trialists attempted to identify if one or more of the components of DBT was more important than another one, each trial arm was too small to be reliable, and any possible differences may have been masked because children in all arms used an alarm as well (Bollard 1982a).

Two trials included a drug in one comparison arm ‐ imipramine (Iester 1991) and desmopressin (Fera 2004). Imipramine seemed to be less effective than an intervention involving retention control training, waking and parental reassurance with and without extra supportive counselling and education, but there were high non‐compliance rates in the two groups without the extra supportive counselling and education. Desmopressin seemed to be better than an assortment of behaviour modification strategies (Fera 2004). However, both drugs stop working after treatment finishes (Glazener 2002; Glazener 2003a).

Adverse effects

Although there were no adverse effects reported in the trials, some did comment on high dropout rates or low compliance rates attributed to the demanding nature of the intervention or the family disruption caused.

Costs

None of the trials gave information about the relative costs of the interventions. However, the question appears to be whether to supplement alarm treatment with DBT, FSHT or another educational intervention, and how best to deliver this. The time needed to teach families in the clinic represents a considerable use of resources, as does frequent follow up and monitoring. Some of the included trials have attempted to reduce this by using filmed, book‐based or multimedia methods of providing information, or by providing the information in different settings or to different recipients, or carrying out some support and follow up by telephone. The trials were too small to evaluate the effectiveness of these different approaches. However, there was a suggestion that extra direct support from a therapist might enhance the effectiveness of an intervention. This would have implications for higher resource use.

Overall completeness and applicability of evidence

Follow up and dropout

Only 7 of the 16 included trials provided longer term results after treatment was finished. This is a serious shortcoming of the research, as continued effectiveness is the main aim of treatment. However, in some cases, it reflected the clinical situation in which families whose children continue to wet the bed ask for alternative treatment. In two trials there was differential dropout from the groups, but an intention‐to‐treat analysis, treating the dropouts as failures, was possible in both cases (Bollard 1981; Iester 1991).

Organic causes and daytime wetting

It is likely that the underlying pathologies of night‐only (monosymptomatic) bedwetting and mixed night and day (diurnal) wetting differ. Those with diurnal wetting are more likely to have an organic cause for their problem, and may be less likely to respond to treatment unless the underlying disease is treated (Jarvelin 1989; Jarvelin 1990). The focus of the review was on monosymptomatic nocturnal enuresis, and all the trials except one (Caceres 1982) excluded either children with daytime wetting or, more importantly, organic causes. To have included only the six trials which explicitly excluded all children with daytime wetting would have limited the review. The results should be interpreted with this in mind.

Settings for treatment

Most of the included trials recruited children from enuresis clinics or were hospital based. Participating families may be especially motivated to tackle the bedwetting. In addition, strict inclusion and exclusion criteria have been imposed in many of the trials. Consequently, the children involved are not necessarily representative of the wider population of those who wet the bed. No trials included children who were learning disabled or from residential homes, although the DBT method was originally developed for adults in those settings.

Quality of the evidence

The 18 trials included in this review were generally small or of poor quality. The average number of children per trial (65) was lower than normal in Cochrane reviews (Mallett 2002). The lack of a sufficiently large sample can result in failure to detect a real treatment difference (because the confidence intervals are wide), or conversely, finding an exaggerated difference to be statistically significant by chance. Only one trial used an adequate method of concealment of allocation to group (Redsell 2003). Despite using this secure method, the trialists reported that there were baseline differences between the groups: there were also baseline differences in two other trials which did not give details of the method of randomisation (Bollard 1982b; Houts 1987a). Three other trials used a quasi‐randomised method with inadequate concealment of allocation. Two studies failed to provide useable data and in three others estimates of variability such as standard deviations were not provided.

Authors' conclusions

Implications for practice.

Although DBT and FSHT were better than no treatment when used in combination with an alarm, there was insufficient evidence to support their use without an alarm. An alarm on its own was also better than DBT on its own, but there was some evidence that combining an alarm with DBT was better than an alarm on its own, suggesting that DBT may augment the effect of an alarm. There was some evidence that direct contact with a therapist might enhance the effects of an intervention (compared with filmed, book‐based or multimedia teaching) but this would have implications for higher use of resources. Both alarm interventions and complex interventions such as DBT involve time and commitment from families and therapists if they are to succeed.

Implications for research.

The use of small samples may obscure treatment effects. Many of the comparisons, especially between different types of training or components of interventions, were conducted in single trials using small samples. Studies investigating the merit of for example, supervision need to be repeated using samples whose size has been determined using power calculations.

Further research on complex or educational interventions for enuresis must incorporate comparisons with other proven methods of management, especially desmopressin, alarms and simple behavioural interventions such as waking and reward systems. Any trials should address the issue of whether benefit is sustained after stopping treatment.

Such trials should focus on children without organic causes of bedwetting, and should include adequate assessment of baseline levels of wetting. They should use uniform outcome measures such as: the number of wet nights during treatment and after the end of treatment; the number achieving 14 consecutive dry nights; adverse effects; acceptability of treatment; compliance; and especially relapse rates after treatment.

The trials should include children from a variety of backgrounds and populations in order to increase the generalisability of the results. Although not studied in the included trials, it has been suggested that not all interventions are suitable for all children. Further research is needed to determine which interventions are appropriate for which groups and in which circumstances in order to guide the choice of treatment.

Children with daytime wetting or symptoms such as urgency are more likely to have a specific pathology such as bladder dysfunction or urinary tract infections. Alternative managements for daytime urinary incontinence need to be covered in a separate Cochrane Review.

What's new

Date Event Description
5 May 2008 New search has been performed Minor update for Issue 3 2008: no new trials identified.

History

Protocol first published: Issue 1, 2004
 Review first published: Issue 1, 2004

Date Event Description
13 September 2005 New search has been performed Minor update for Issue 1 2006: two new trials added (Fera 2004 and van Kampen 2005), but the conclusions of the review were unchanged.
26 November 2003 New citation required and conclusions have changed Review first published: Issue 1 2004

Acknowledgements

An earlier version of this review was originally part of that written for the National Health Service Centre for Reviews and Dissemination, University of York, by Deborah Lister‐Sharp, Susan O'Meara, Matthew Bradley and Trevor A Sheldon (Lister‐Sharp 1997). It is published as: A Systematic Review of the Effectiveness of Interventions for Managing Childhood Nocturnal Enuresis. The York review obtained information from a variety of sources, including organisations, manufacturers and individuals. These are listed in Appendix 2 pp 83 to 88 of that review. We would also like to thank the Consumer Network at the Australasian Cochrane Centre for help with the synopsis.

Data and analyses

Comparison 1. Complex interventions versus no‐treatment controls.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Mean number of wet nights per week on treatment 2   Mean Difference (IV, Fixed, 95% CI) Subtotals only
1.1 DBT + alarm vs control 2 43 Mean Difference (IV, Fixed, 95% CI) ‐4.09 [‐5.44, ‐2.74]
2 Mean number of wet nights per week on treatment (no SDs)     Other data No numeric data
2.1 DBT (office training of parent and child, no alarm) vs control     Other data No numeric data
2.2 DBT (home training of parent and child, no alarm) vs control     Other data No numeric data
2.3 DBT (office training of parent only, no alarm) vs control     Other data No numeric data
2.4 DBT with alarm vs control     Other data No numeric data
2.5 DBT without alarm vs control     Other data No numeric data
3 Number not achieving 14 consecutive dry nights 5   Risk Ratio (M‐H, Fixed, 95% CI) Subtotals only
3.1 DBT (alarm + therapist at home) vs control 1 40 Risk Ratio (M‐H, Fixed, 95% CI) 0.03 [0.00, 0.42]
3.2 DBT (alarm + therapist in hosp) vs control 1 40 Risk Ratio (M‐H, Fixed, 95% CI) 0.03 [0.00, 0.42]
3.3 DBT (alarm + parents as therapists at home) vs control 1 40 Risk Ratio (M‐H, Fixed, 95% CI) 0.03 [0.00, 0.42]
3.4 DBT + alarm vs control 4 143 Risk Ratio (M‐H, Fixed, 95% CI) 0.19 [0.12, 0.30]
3.5 FSHT + alarm vs control 1 24 Risk Ratio (M‐H, Fixed, 95% CI) 0.34 [0.16, 0.72]
3.6 DBT without alarm vs control 2 60 Risk Ratio (M‐H, Fixed, 95% CI) 0.82 [0.66, 1.03]
4 Number failing or relapsing 2   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
4.1 DBT (alarm + therapist at home) vs control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.2 DBT (alarm + therapist in hospital) vs control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.3 DBT (alarm + parents as therapists at home) vs control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.4 DBT with alarm vs control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.5 FSHT with alarm vs control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.6 DBT without alarm vs control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]

Comparison 2. Complex interventions alone versus other behavioural interventions.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Mean number of wet nights per week on treatment (no SDs)     Other data No numeric data
1.1 DBT vs alarm     Other data No numeric data
1.2 DBT vs DBT + alarm     Other data No numeric data
2 Number not achieving 14 consecutive dry nights 4   Risk Ratio (M‐H, Fixed, 95% CI) Subtotals only
2.1 DBT (no alarm) vs alarm 2 54 Risk Ratio (M‐H, Fixed, 95% CI) 4.56 [1.90, 10.91]
2.2 DBT (no alarm) vs DBT + alarm 2 100 Risk Ratio (M‐H, Fixed, 95% CI) 24.73 [6.25, 97.85]
2.3 retention control training + wakening + parental reassurance vs same + counselling + educational reinforcement 1 132 Risk Ratio (M‐H, Fixed, 95% CI) 2.13 [1.11, 4.11]
3 Number failing or relapsing 3   Risk Ratio (M‐H, Fixed, 95% CI) Subtotals only
3.1 DBT (no alarm) vs alarm 1 40 Risk Ratio (M‐H, Fixed, 95% CI) 1.7 [1.06, 2.73]
3.2 DBT (no alarm) vs DBT + alarm 2 100 Risk Ratio (M‐H, Fixed, 95% CI) 2.81 [1.80, 4.38]
3.3 retention control training + wakening + parental reassurance vs same + counselling + educational reinforcement 1 132 Risk Ratio (M‐H, Fixed, 95% CI) 2.07 [1.16, 3.72]

2.1. Analysis.

Comparison 2 Complex interventions alone versus other behavioural interventions, Outcome 1 Mean number of wet nights per week on treatment (no SDs).

Mean number of wet nights per week on treatment (no SDs)
Study Complex Other
DBT vs alarm
Bollard 1981 Mean 3.8 wet nights (n=20) 
 (Group D including dropouts) Mean 0.6 wet nights (n=20) 
 (Group E)
DBT vs DBT + alarm
Bollard 1981 Mean 3.8 wet nights (n=20) 
 (Group D including dropouts) Mean 0 wet nights (n=60) 
 (Groups A+B+C)
Bollard 1982b Mean 3.25 wet nights (n=10) Mean 0.2 wet nights (n=10)

2.2. Analysis.

2.2

Comparison 2 Complex interventions alone versus other behavioural interventions, Outcome 2 Number not achieving 14 consecutive dry nights.

Comparison 3. Supplemented complex interventions versus other behavioural interventions.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Mean number of wet nights per week on treatment 2   Mean Difference (IV, Fixed, 95% CI) Subtotals only
1.1 DBT + alarm vs alarm 2 43 Mean Difference (IV, Fixed, 95% CI) ‐1.78 [‐3.28, ‐0.28]
1.2 DBT + alarm vs PFMT 1 22 Mean Difference (IV, Fixed, 95% CI) ‐1.85 [‐5.36, 1.66]
2 Mean number of wet nights per week on treatment (no SDs)     Other data No numeric data
2.1 DBT + alarm vs alarm     Other data No numeric data
3 Number not achieving 14 consecutive dry nights 6   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
3.1 DBT + alarm vs alarm 5   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.2 DBT + alarm vs PFMT 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.3 FSHT + alarm vs alarm 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.4 FSHT + alarm vs alarm + retention control training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
4 Mean number of wet nights per week at follow up 1   Mean Difference (IV, Fixed, 95% CI) Totals not selected
4.1 DBT + alarm vs alarm 1   Mean Difference (IV, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.2 DBT + alarm vs PFMT 1   Mean Difference (IV, Fixed, 95% CI) 0.0 [0.0, 0.0]
5 Number failing or relapsing 4   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
5.1 DBT + alarm vs alarm 3   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
5.2 FSHT + alarm vs alarm 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
5.3 FSHT + alarm vs alarm + retention control training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]

3.1. Analysis.

3.1

Comparison 3 Supplemented complex interventions versus other behavioural interventions, Outcome 1 Mean number of wet nights per week on treatment.

3.2. Analysis.

Comparison 3 Supplemented complex interventions versus other behavioural interventions, Outcome 2 Mean number of wet nights per week on treatment (no SDs).

Mean number of wet nights per week on treatment (no SDs)
Study Complex + other Other
DBT + alarm vs alarm
Bollard 1981 Mean 0 wet nights (n=60) 
 (Groups A+B+C) Mean 0.6 wet nights (n=20) 
 (Group E)
Butler 1988 Mean 1.05 wet nights (n=35) Mean 1.81 wet nights (n=28)
Butler 1990 Mean 1.79 wet nights (n=24) Mean 1.56 wet nights (n=24)

3.4. Analysis.

3.4

Comparison 3 Supplemented complex interventions versus other behavioural interventions, Outcome 4 Mean number of wet nights per week at follow up.

3.5. Analysis.

3.5

Comparison 3 Supplemented complex interventions versus other behavioural interventions, Outcome 5 Number failing or relapsing.

Comparison 4. Sensitivity analysis: supplemented complex interventions versus other behavioural interventions.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Number not achieving 14 consecutive dry nights 4   Risk Ratio (M‐H, Fixed, 95% CI) Subtotals only
1.1 DBT + alarm vs alarm 4 186 Risk Ratio (M‐H, Fixed, 95% CI) 0.60 [0.38, 0.94]
2 Number failing or relapsing 2   Risk Ratio (M‐H, Fixed, 95% CI) Subtotals only
2.1 DBT + alarm vs alarm 2 104 Risk Ratio (M‐H, Fixed, 95% CI) 0.5 [0.31, 0.80]

Comparison 5. Complex interventions ‐ different training regimens.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Mean number of wet nights per week on treatment (no SDs)     Other data No numeric data
1.1 therapist at home vs therapist in hospital     Other data No numeric data
1.2 therapist at home vs parent as therapist at home     Other data No numeric data
1.3 therapist in hospital vs parent as therapist at home     Other data No numeric data
1.4 teaching for parent and child in hospital vs teaching for parent only in hospital     Other data No numeric data
1.5 teaching for parent and child in hospital vs teaching for parent and child at home     Other data No numeric data
1.6 teaching for parent and child at home vs teaching for parent only in hospital     Other data No numeric data
2 Number not achieving 14 consecutive dry nights 4   Risk Ratio (M‐H, Fixed, 95% CI) Subtotals only
2.1 therapist at home vs therapist in hospital 1 40 Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.2 therapist at home vs parent as therapist at home 1 40 Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.3 therapist in hospital vs parent as therapist at home 1 40 Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.4 teaching for parent and child in hospital vs teaching for parent only in hospital 1 14 Risk Ratio (M‐H, Fixed, 95% CI) 0.33 [0.02, 7.02]
2.5 teaching for parent and child in hospital vs teaching for parent and child at home 1 16 Risk Ratio (M‐H, Fixed, 95% CI) 0.14 [0.01, 2.22]
2.6 teaching for parent and child at home vs teaching for parent only in hospital 1 16 Risk Ratio (M‐H, Fixed, 95% CI) 3.11 [0.44, 22.00]
2.7 FSHT live delivery vs FSHT filmed delivery 2 51 Risk Ratio (M‐H, Fixed, 95% CI) 0.36 [0.15, 0.90]
3 Number failing or relapsing 3   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
3.1 therapist at home vs therapist in hospital 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.2 therapist at home vs parent as therapist at home 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.3 therapist in hospital vs parent as therapist at home 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.4 teaching for parent and child in hospital vs teaching for parent only in hospital 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.5 teaching for parent and child in hospital vs teaching for parent and child at home 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.6 teaching for parent and child at home vs teaching for parent only in hospital 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.7 FSHT live delivery vs FSHT filmed delivery 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]

5.1. Analysis.

Comparison 5 Complex interventions ‐ different training regimens, Outcome 1 Mean number of wet nights per week on treatment (no SDs).

Mean number of wet nights per week on treatment (no SDs)
Study Complex 1 Complex 2
therapist at home vs therapist in hospital
Bollard 1981 Mean 0 wet nights (n=20) Mean 0 wet nights (n=20)
therapist at home vs parent as therapist at home
Bollard 1981 Mean 0 wet nights (n=20) Mean 0 wet nights (n=20)
therapist in hospital vs parent as therapist at home
Bollard 1981 Mean 0 wet nights (n=20) Mean 0 wet nights (n=20)
teaching for parent and child in hospital vs teaching for parent only in hospital
Keating 1983 Mean 2.7 wet nights (n=7) Mean 1.9 wet nights (n=7)
teaching for parent and child in hospital vs teaching for parent and child at home
Keating 1983 Mean 2.7 wet nights (n=7) Mean 2.5 wet nights (n=7)
teaching for parent and child at home vs teaching for parent only in hospital
Keating 1983 Mean 2.5 wet nights (n=7) Mean 1.9 wet nights (n=7)

5.3. Analysis.

5.3

Comparison 5 Complex interventions ‐ different training regimens, Outcome 3 Number failing or relapsing.

Comparison 6. Comparing components of complex interventions.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Mean number of wet nights per week on treatment (no SDs)     Other data No numeric data
1.1 alarm + waking VS alarm + retention control training     Other data No numeric data
1.2 alarm + waking VS alarm + positive practice+ cleanliness training     Other data No numeric data
1.3 alarm + waking VS alarm + waking + retention control training     Other data No numeric data
1.4 alarm + waking VS alarm + waking + positive practice + cleanliness training     Other data No numeric data
1.5 alarm + waking VS alarm + retention control training + positive practice + cleanliness training     Other data No numeric data
1.6 alarm + retention control training VS alarm + positive practice+ cleanliness training     Other data No numeric data
1.7 alarm + retention control training VS alarm + waking + retention control training     Other data No numeric data
1.8 alarm + retention control training VS alarm + waking + positive practice + cleanliness training     Other data No numeric data
1.9 alarm + retention control training VS alarm + retention control training + positive practice + CT     Other data No numeric data
1.10 alarm + positive practice + cleanliness VS alarm + waking + retention control training     Other data No numeric data
1.11 alarm + positive practice + cleanliness VS alarm + waking + positive practice + cleanliness training     Other data No numeric data
1.12 alarm + positive practice + cleanliness training VS alarm + retention control training + PP + CT     Other data No numeric data
1.13 alarm + waking + retention control training VS alarm + waking + positive practice + cleanliness training     Other data No numeric data
1.14 alarm + waking + retention control training VS alarm + retention control training + positive practice + CT     Other data No numeric data
1.15 alarm + waking + positive practice + cleanliness training VS alarm + retention control training + PP + CT     Other data No numeric data
2 Number not achieving 14 dry nights 1   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
2.1 alarm + waking VS alarm + retention control training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.2 alarm + waking VS alarm + positive practice+ cleanliness training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.3 alarm + waking VS alarm + waking + retention control training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.4 alarm + waking VS alarm + waking + positive practice + cleanliness training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.5 alarm + waking VS alarm + retention control training + positive practice + cleanliness training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.6 alarm + retention control training VS alarm + positive practice+ cleanliness training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.7 alarm + retention control training VS alarm + waking + retention control training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.8 alarm + retention control training VS alarm + waking + positive practice + cleanliness training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.9 alarm + retention control training VS alarm + retention control training + positive practice + CT 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.10 alarm + positive practice + cleanliness VS alarm + waking + retention control training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.11 alarm + positive practice + cleanliness VS alarm + waking + positive practice + cleanliness training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.12 alarm + positive practice + cleanliness training VS alarm + retention control training + PP + CT 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.13 alarm + waking + retention control training VS alarm + waking + positive practice + cleanliness training 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.14 alarm + waking + retention control training VS alarm + retention control training + positive practice + CT 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.15 alarm + waking + positive practice + cleanliness training VS alarm + retention control training + PP + CT 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]

Comparison 7. Complex interventions versus drugs.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Number not achieving 14 consecutive dry nights 2   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
1.1 3‐step (retention control training + wakening + parental reassurance) VS imipramine 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
1.2 3‐step intervention + counselling + educational reinforcement VS imipramine 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
1.3 Toileting, alarm clock, pelvic floor training, dietary and fluid adjustment etc VS desmopressin 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2 Mean number of wet nights per week on treatment 1   Mean Difference (IV, Fixed, 95% CI) Subtotals only
2.1 Toileting, alarm clock, pelvic floor training, dietary and fluid adjustment etc VS desmopressin 1 30 Mean Difference (IV, Fixed, 95% CI) 1.67 [0.35, 2.99]
3 Number failing or relapsing 1   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
3.1 3‐step (retention control training + wakening + parental reassurance) VS imipramine 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
3.2 3‐step (RCT+ wakening + parental reassurance) + counselling + educational reinforcement VS imipramine 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]

7.1. Analysis.

7.1

Comparison 7 Complex interventions versus drugs, Outcome 1 Number not achieving 14 consecutive dry nights.

Comparison 8. Educational interventions versus no‐treatment controls.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Number not achieving 14 consecutive dry nights 1   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
1.1 Enuresis information on interactive CD‐rom vs no treatment control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
1.2 Written enuresis information vs no treatment control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2 Number failing or relapsing 1   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
2.1 Enuresis information on interactive CD‐rom vs no treatment control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2.2 Written enuresis information vs no treatment control 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]

8.1. Analysis.

8.1

Comparison 8 Educational interventions versus no‐treatment controls, Outcome 1 Number not achieving 14 consecutive dry nights.

Comparison 9. Different educational interventions compared.

Outcome or subgroup title No. of studies No. of participants Statistical method Effect size
1 Number not achieving 14 consecutive dry nights 1   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
1.1 Enuresis information on interactive CD‐rom vs written enuresis information 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]
2 Number failing or relapsing 1   Risk Ratio (M‐H, Fixed, 95% CI) Totals not selected
2.1 Enuresis information on interactive CD‐rom vs written enuresis information 1   Risk Ratio (M‐H, Fixed, 95% CI) 0.0 [0.0, 0.0]

9.1. Analysis.

9.1

Comparison 9 Different educational interventions compared, Outcome 1 Number not achieving 14 consecutive dry nights.

Characteristics of studies

Characteristics of included studies [ordered by study ID]

Azrin 1974.

Methods RCT ‐ coin flip used to randomise each of pairs of children 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting: Not mentioned
Setting: children who responded to a newspaper advertisement for enuretics
Participants No. of children (boys): 26 (19) 
 Exclusion: medical causes 
 Ages: 3+, mean 8 years 
 Baseline frequency 7 days/week.
Interventions Expt 1 
 A (7): DBT (parent‐and‐child alarm; PP; W; increasing fluid intake; rewards; CT; training in inhibiting urination (? retention control training) 
 B (7): Child‐only alarm for first 2 weeks only (then DBT) 
 Expt 2 
 C (6): DBT, parent‐only alarm 
 D (6): Child‐only alarm
Duration of treatment: 2 weeks (then all groups received DBT + Alarm)
Follow up: 6 months
Outcomes Fewer wet nights in first 2 weeks with A+C (median 1 vs B+D 5 in second week, P<0.005). 
 More children achieving 6 dry nights in A
Notes Pairs matched for age, sex and frequency of wetting 
 No useable data.
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? High risk C ‐ Inadequate

Azrin 1978.

Methods RCT (details not given) 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Yes
Participants No. of children (boys): 55 (41) 
 Inclusion: Age at least 3 years; no daytime wetting; wetting at least 4 times per week; able to understand instructions; medical examination and treatment
Age: mean 7 years (range 3‐14) (20 less than 6 years) 
 Baseline wetting: 91% of nights
Interventions A (28): Intensive DBT (PP, CT) plus rehearsing during the day with increased fluid intake, stream interruption exercises, Retention Control Training, repeated awakening, rewards for dry nights or compliance but NO ALARM 
 B (27): Alarm (pad‐and‐buzzer) 
 Duration of trial: 2 weeks, after which parents could swap to other arm
Outcomes Per cent wet nights during 2 weeks: A, 15%; B, 76% 
 No. of children swapping to other group after 2 weeks: A, 0/27; B, 23/27
Notes Comparability of groups at baseline not reported 
 No FU possible after 2 weeks 
 No SDs 
 Very young children (20 under age 6 years) included
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Bennett 1985.

Methods RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Not mentioned 
 Daytime wetting: excluded if significant
Participants No. of children (boys): 40 (25) 
 Dropouts: 32 (A,9; B,11; C,10; D,3) 
 Inclusion: primary nocturnal enuresis, referred to enuresis service by GP, negligible daytime wetting 
 Exclusion: encopresis, previous behavioural intervention, gross psychopathology 
 Age mean 8.5 years (SD 3.2) range 5‐12 
 Baseline wetting: dry nights, boys 3/14; girls 2.4/14
Interventions A: (9) Alarm (pad and buzzer) 
 B: (12) Stop‐start training (sphinchter muscle exercises, bladder training) 
 C: (10) Dry Bed Training including alarm 
 D: (9) Waiting list control (used star chart after first dry night) 
 Duration of treatment: 10 weeks
Outcomes Mean dry nights in last 2 weeks of 12 weeks treatment: A, 12 (SD 3.9); B, 7.5 (5.2); C, 11.2 (3.6); D, 3.7 (3.0) 
 No. achieving 14 dry nights: 
 A, 4/9; B, 2/12; C, 5/10; D, 0/9 
 Mean dry nights at followup: 
 A, 12.3 (3.1); B, 7.1 (5.8); C, 9.3 (5.3). (D treated after 12 weeks) 
 Adverse events: not mentioned
Notes All children got star charts after their first dry night 
 High dropout rate
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Bollard 1981.

Methods Experiment 2 
 RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: No 
 Analysed on intention to treat basis and with dropouts excluded
Participants Experiment 2 
 Number of children: 100 
 No. of boys: A:14 B:13 C:16 D:14 E:14 F:11 
 No. of dropouts: 12 from D
Inclusion: thorough medical examination; regularly wetting at least one night per week; no other treatment during trial 
 Previous treatment: no details 
 Mean age (years): A:9.3 B:8.11 C:9.7 D:8.6 E:8.8 F:8.10
Baseline wetting: mean number of wet nights: A:5.8 B:5.2 C:6.0 D:5.7 E:6.0 F:4.7
Interventions Experiment 2 
 A (20): DBT (A + W + CT + PP) with therapist at home 
 B (20): DBT (A + W + CT + PP) with therapist at hospital 
 C (20): DBT (A + W + CT + PP) with parents as therapists at home 
 D (20): DBT (W + CT + PP) with parents as therapists at home WITHOUT enuresis alarm. 
 E (20): alarm 
 F (20): waiting list control
Duration of treatment: until 14 consecutive dry nights or 20 weeks
FU at 3, 6 and 12 months
Outcomes Experiment 2 
 Comparing DBT with alarm only ‐ DBT significantly more effective in terms of number of wet nights and days to dryness
Mean number of wet nights per week at end of week 20 
 (incl dropouts) A:0, B:0, C:0, D: (n=20) 3.8, E: 0.6, F: 4.4 
 (excl dropouts) A:0, B:0, C:0, D:(n=8) 1.3, E:0.6, F:4.4
No. achieving 14 consecutive dry nights: A:20, B:20, C:20, D:5, E:16, F:2 
 (p < 0.05)
No. relapsing: A:5, B:6, C:4, D:2, E:6, F:2 NS
ie no. failing or relapsing: A: 5/20, B: 6/20, C: 4/20, D: 17/20, E: 10/20, F: 20/20
Notes Experiment 2 
 No details of blinding 
 DBT no alarm group (D) younger than others and 
 more girls in waiting list control group (F) 
 No SDs
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Bollard 1982a.

Methods Mainly RCT but also comparison with previous study [A] and [H] from another study 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Not mentioned
Participants No. of children (2 groups combined) (boys): 127 (88) 
 Inclusion: no underlying organic pathology
Previous treatment: many had previously sought help but none undergoing any form of enuresis related drug or psychotherapy at the time of the study. 
 Mean age: 9 years 10 months 
 Baseline wetting: Overall mean number of wet nights per week = 5.5
Interventions [A (35): alarm only (A)] 
 B (12): alarm (A) + waking schedule (W) 
 C (12): A+retention control training 
 D (12): A+ positive practice (PP)+ cleanliness training (CT) 
 E (12): A+W+retention control training
F (12): A+W+PP +CT 
 G (12): A+retention control training+PP +CT 
 [H (20): Full DBT] 
 Duration of treatment: 20 weeks 
 Follow up: none
Outcomes Mean no. of wet nights during 20 week treatment period: 
 A: 27 B: 13 C: 24 D: 23 E: 14 F: 10 G: 21 H: 11
Number of cases becoming dry: A: 31 B: 12 C: 11 D: 10 E: 12 F: 12 G: 11 H: 20
Significant difference in response rate of group with waking schedule vs those without (Chi squared = 13.04, df = 3, p < 0.01)
Notes Groups A and H from another trial, data not used 
 No analysis of comparability of groups 
 No blinding 
 No SDs 
 No follow up
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Bollard 1982b.

Methods RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: not mentioned
Participants Number of children (boys): 30 (18) 
 No. dropouts: 0
Inclusion: at least 1 wet night/week; no underlying pathology
Previous treatment: none current
Mean ages: A:8 years 5 months B:9 years 4 months C:9 years 5 months 
 Baseline wetting: mean number of wet nights per week: A: 4.9 B: 5.0 C: 5.3
Interventions J (10): DBT + A (enuresis alarm) 
 K (10): DBT WITHOUT alarm 
 L (10): Control (no treatment)
Duration of treatment: until 14 dry nights or maximum of 8 weeks
Follow up after 3 months
Outcomes Mean no. of wet night per week (final week): J:0.2 K:3.25 L:5.3 
 No. of children achieving 14 consecutive dry nights: J: 9/10 K: 2/10 L: 0/10 
 (P= 0.01) 
 No. relapsing: J:3/10 K:4/10
Ultimately 30 children underwent DBT with alarm and 29 achieved success criterion within 16 weeks 
 (Subsequent treatment with DBT + alarm for K & L resulted in similar outcomes (9/10 and 10/10 cured))
Notes Groups comparable at baseline 
 Results estimated from graph 
 No SDs 
 1 failure not included in analysis 
 Small sample size 
 No details of previous treatment
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Butler 1988.

Methods CCT (alternate allocation) 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Not mentioned
Participants No. of children: originally 74 but 11 excluded after baseline assessments (A: 18 B: 29)
Inclusion: age at least 6 years;wetting at least five nights a week for a month; normal clinical exam; normal urine on microscopy; normal intelligence (assessed by reference to educational background and parental‐child interview); not having any form of enuresis related drug or psychotherapeutic treatment
Previous treatment: 36 (48.6%) enuresis alarm
Mean age: A: 8.99 B: 9.86
Baseline wetting: mean number of dry nights during 4 weeks 
 A: 1.07 B: 1.02
Interventions A (28): Standard enuresis alarm treatment (A) 
 B (35): Modified DBT + alarm (A + W + PP + retention control training) WITHOUT reprimands during CT 
 Duration of treatment: 16 weeks 
 No Follow up
Outcomes Mean number of dry nights in last 4 weeks 
 A:20.76 B:23.79 F(1,46) = 1.77 
 Number of children achieving 14 dry night criterion 
 A:20/28 (71%) B: 25/35 (71%) no significant difference
Mothers in dropout group significantly more angry with bedwetting than other groups
Notes No significant difference between groups for demographic factors but Group B more likely to have previously used alarm 
 Analysis of covariance adjusted for the effects of previous experience with enuresis alarm 
 No blinding 
 Not intention to treat
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? High risk C ‐ Inadequate

Butler 1990.

Methods Experiment 2 
 CCT (alternate allocation) 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Yes
Participants Experiment 2 
 No. of children (boys): 48 (39) 
 Number of dropouts: A: 2 B 1 
 Inclusion: wetting at least 4 nights a week for a month; nomal physical examination; normal urine microscopy; normal intelligence (assessed by reference to educational background and parent\child interview); no associated diurnal enuresis
Previous treatment: failed with pad and bell alarm
Mean age (years): A: 10.2 B: 11.2 
 Severity at baseline: mean number of DRY nights per week: A: 1.2 B: 1.3
Interventions Experiment 2 
 A (24): Modified DBT + alarm (A + W + retention control training) 
 B (24): body‐worn alarm (A)
Duration of treatment: 16 weeks 
 Follow up after 6 months
Outcomes Experiment 2 
 Mean number of wet nights in 16 weeks 
 A: 28.7 B: 25.0
Number (%) attaining 14 consecutive dry nights 
 A: 14 (58) B: 20 (83)
Mean number of wet nights to achievement of 14 consecutive dry nights 
 A: 53.7 B: 40.7
Number (%) children relapsing: A: 7 (50) B: 9 (45)
(ie fail or relapse: A: 17/24, B: 13/24)
Notes Experiment 2 
 Groups did not differ significantly on any variable 
 Unclear if intention to treat analysis 
 No SDs
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? High risk C ‐ Inadequate

Caceres 1982.

Methods RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: No 
 Daytime wetting excluded: No
Participants No. of children (boys): 14 (9) 
 Inclusion: enuresis, or behaviour problem + enuresis. Some were not daytime toilet trained 
 Previous treatment: all had failed with psychotherapy, drugs or fluid restriction 
 Age: mean 9 years (range 6‐14) 
 Baseline wetting: every night
Interventions A (7): Enuresis alarm (Mowrer's pad‐and‐bell) 
 B (7): DBT (but WITHOUT alarm) + rewards
Duration of treatment: 1 month, then crossed over to other arm if not 50% improved
Outcomes Not cured on original treatment: A: 0/7, B: 5/7
Adverse effects: parents of 2 children from Group A refused to transfer to Group B because of practical difficulties, and 1 from Group B could not transfer to A because of the risk of the alarm waking the neighbours
Notes Children crossed over to alternative treatment if not successful (5 of B group changed to A). Cure rates given while on first treatment.
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Fera 2004.

Methods RCT (randomized in 2 groups) 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: No 
 Daytime wetting excluded: Yes 
 Setting: Federal University of Sao Paulo
Participants No. of children (boys): 30 (21) 
 Dropouts: None 
 Inclusion: monosymptomatic nocturnal enuresis, age over 5 years, no daytime wetting 
 Exclusion: none mentioned 
 Previous treatment: none 
 Age, mean years (SD): 9.23 (1.85) 
 Baseline wetting, mean (SD) wet nights in 2 weeks: 9.40 (3.40)
Interventions A (15): DDAVP (desmopressin), titrated to maximum 0.4 mg at bedtime 
 B (15): behavioural modification (dietary and fluid adjustment, voiding schedules, double voiding, bedtime toileting, alarm clock once at night, pelvic floor training, environmental modifications, changes in parents' attitudes, improvement of self‐esteem, self care) 
 Duration of treatment: 30 days 
 Follow up: none
Outcomes Wet nights during last 2 weeks of treatment N, mean (SD): A: 15, 7.27 (4), B: 15, 3.93 (3.32) 
 50% improvement: A: 7/15, B: 8/15 
 Complete failure: A: 5/15, B: 1/15 
 Adverse effects: not mentioned
Notes Groups comparable at baseline on age, gender and baseline wetting 
 No data for children 'cured' (14 consecutive dry nights)
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Houts 1986.

Methods RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: No 
 Daytime wetting excluded: not mentioned 
 Setting: media recruitment and paediatric referrals
Participants No. of children (boys): 45 (35) 
 Dropouts: A: 2, B: 2, C: 3 
 Inclusion: Primary enuresis 
 Age 5‐13 years 
 Baseline wetting: mean 5.41 (SD 1.63) wet nights/week
Interventions A (15): Enuresis alarm + over‐learning + retention control training (Full Spectrum Home Training Package) 
 B (15): Enuresis alarm + retention control training 
 C (15): Enuresis alarm alone 
 D (11): Waiting list control 
 Duration of treatment: 16 weeks 
 Follow up: 1 year
Outcomes A: cured 9, failed 4, dropout 2; B: cured 13, dropped out 2; C: cured 9, failed 3, dropped out 3; D none cured (11/11 failed) 
 Relapse at end of study after retreatment if necessary: A: 1, B: 6, C: 3 
 ie. failed or relapsed: A 5/13, B: 6/13, C: 6/12
Notes Groups comparable at baseline 
 A, B + C received 1 hour group training and CT 
 Relapses were retreated with initial treatment allocated 
 Children who failed were older, and dropouts were younger
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Houts 1987a.

Methods RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: No 
 Daytime wetting excluded: Yes
Setting: media advertising and referral from physicians
Participants Study 1 
 No. of children: 40 
 Inclusion: primary enuresis, no daytime wetting
Interventions Study 1 
 A (10): Immediate live delivery of FSHT 
 B (10): Immediate filmed delivery of FSHT 
 C (10): Baseline recording for 16 weeks then live delivery FSHT 
 D (10): Baseline recording for 16 weeks then filmed delivery of FSHT
Duration of treatment: 16 weeks 
 Follow up: 1 year
Outcomes Study 1 
 A+C (live): 15/20 success, 4/20 failed, 1/20 dropped out (4/19 failed ) 
 B+D (filmed): 6/20 success, 7/20 failed, 7/20 dropped out (7/14 failed) 
 Relapse rate 3 in each group. 
 Failure + relapse rate: A+C (live) 7/19, B+D (filmed) 10/14.
Notes Study 1 had 2x2 factorial design with 'baseline waiting' for half the group. This had no effect on outcome, therefore results presented combined. 
 More girls and higher baseline wetting in live delivery group
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Houts 1987b.

Methods RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: No 
 Daytime wetting excluded: Yes
Setting: media advertising and referral from physicians
Participants Study 2 
 No. of children: 24 
 Inclusion: primary enuresis, no daytime wetting
Interventions Study 2 
 E (12): Immediate live delivery of FSHT + waking 
 F (12): Immediate filmed delivery of FSHT
Outcomes Study 2 
 E (live): 5/12 success, 1/12 failed, 5/12 did not attend (ie 1/7 failed) 
 F (filmed): 4/12 success, 6/12 failed, 1/12 did not attend (ie 6/11 failed)
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Iester 1991.

Methods RCT (randomly divided with computer) 
 Systematic baseline measure of wetting: No 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Not mentioned
Participants No. of children: 168 
 Inclusion: functional enuresis 
 Exclusion: organic causes, emotional disturbance 
 Previous Rx: none 
 Ages: 6‐11 years
Interventions A (36): 6 weeks with imipramine 0.9‐1.5 mg/kg, max 50mg 
 B (36): 3 step programme: a) reassurance to parents; b) bladder retention training and wakening with alarm clock before micturition; c) parental involvement 
 C (96): Motivational therapy (counselling) + education (computer programme) + 3 step therapy 
 Duration Rx: 6months 
 Follow up: 12 months
Outcomes Failure rates: 
 A: 22/36, B: 12/36, C: 15/96 
 Relapse A: 2, B: 2, C: 3 
 Failure + relapse rates: A: 24/36, B: 14/36, C: 18/96 
 Compliance with Rx: A: 14/36, B: 24/36, C: 81/96
Notes Pad‐and‐bell wetting alarm not used
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Keating 1983.

Methods RCT 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Yes
Participants No. of children (boys):30 (18) 
 Dropouts: none until followup
Inclusion: diurnally continent; child must be able to follow simple instructions; organic factors ruled out by a physician
Previous treatment: no details
Mean age: 8.1 years (range: 4 to 14)
Baseline severity: wet at least 50% of nights
Interventions A (7): DBT with office (hospital) training for parent and child 
 B (9): DBT with in home training for parent and child 
 C (7): DBT with office training for parent only 
 D (7): waiting list control
NO alarms 
 Duration of treatment: 5 weeks 
 Follow up after 5 months
Outcomes Mean number of DRY nights per week in final treatment week 
 A: 4.3 B: 4.5 C: 5.1 D: 5.0
Number of children achieving 14 consective dry nights: A: 7 B: 5 C: 6 NS
Number of children relapsing: A: 2 B: 2 C: 2
No differences among treatment groups in terms of parental self‐reports of consistent supervision and conduct of training following initial instruction, nor differences in terms of parental satisfaction with DBT programme
Notes No significant difference between groups in terms of age.
No blinding 
 No information about control group after 5 weeks 
 Data from graphs 
 No SDs
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Nawaz 2002.

Methods RCT (random allocation to groups following matching on age and sex) 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Yes
Setting: community health centres in Glasgow, Scotland
Participants No. of children (boys): 36 (18) 
 Dropouts: 0
Inclusion: Age 7‐12 years, baseline wetting at least twice per months, attending mainstream school and willing to be randomised
Exclusion: medical, physiological or psychiatric pathology, diurnal enuresis, encopresis
Previous treatment: some, but stopped during trial
Age: Mean 9.9 years (SD 1.83) 
 Baseline wetting: mean 5.67 per week (SD 1.26) for 4 weeks
Interventions A (12): DBT + alarm 
 B (12): alarm only 
 C (12): untreated controls continued recording wet nights for 16 weeks, then offered treatment they preferred 
 A + B also received standardised instrucitons (manual and videotape) and had 2 weekly telephone calls
Duration of treatment: 16 weeks or until 14 dry nights if earlier
Follow up: 6 months
Outcomes Wet nights per week during trial (final week): A: mean 0.83 (SD 1.40), B: 3.25 (2.67), C: 5 (2.26) 
 No. not achieving 14 dry nights: A: 4/12, B: 9/12, C: 11/12 
 No. relapsing after end of trial: A: 1, B: 1 
 Fail or relapse rate: A: 5/12, B: 10/12
Notes Groups comparable on age, sex, baseline wetting and DepCat (deprivation) scores 
 DBT described as: intensive first night, arousing child and taking him to toilet, accident contingencies and normal routine
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk B ‐ Unclear

Redsell 2003.

Methods RCT (cluster randomised controlled trial, stratified on Jarman index, ethnicity and electoral ward) 
 Systematic baseline measure of wetting: Yes 
 Organic causes excluded: No 
 Daytime wetting excluded: Not mentioned
Setting: school nurse‐led enuresis clinics in Leicestershire, UK
Participants No. of children (boys):270 (of 287 eligible) (176) 
 Inclusion: Primary (79%) and secondary (19%) enuresis, re‐referrals 23% 
 Previous treatment: not in last 6 months
Age: mean 7.98 years (SD 2.23) (range 5‐16)
Interventions A (108): multimedia interactive CD‐rom with enuresis information 
 B (87): Leaflets with same information 
 C (75): control, no extra information 
 All children also had 4 weeks baseline assessment with star chart reward system, and received other enuresis treatment as deemed appropriate by their therapists (including alarms in some cases)
Duration of treatment: 6 months 
 Follow up: 6 months
Outcomes No. not achieving 14 dry nights during first 6 months: A: 51/108, B: 46/87, C: 39/75 
 Failure or relapse: A: 87/108, B: 61/87, C: 57/75
Also maternal tolerance scale, impact of bedwetting score
Notes Groups comparable at baseline on age, and clinics comparable on Jarman indices and ethnicity, but postcode analysis showed group A were from a more advantaged population, fewer ethnic minority children 
 Power calculation done a priori 
 Re‐referred children older (mean 9.96 vs 7.38 years)
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Low risk A ‐ Adequate

van Kampen 2005.

Methods RCT (stratified on age) 
 Systematic baseline measure of wetting: No 
 Organic causes excluded: Yes 
 Daytime wetting excluded: Not mentioned 
 Setting: Catholic University, Leuven
Participants No. of children: 63 
 Dropouts: 4 
 Inclusion criteria: nocturnal enuresis 
 Exclusion criteria: not stated 
 Previous treatment: not stated
Interventions A (n not given): FSHT + pelvic floor muscle training (PFMT) 
 B (n not given): FSHT without pelvic floor muscle training 
 Duration of treatment: 6 months
Outcomes Number in groups not given, 88.9% cure rate in whole group at 6 months 
 Authors state: no difference in efficacy or duration of treatment between the groups, and age and baseline motivation predicted success
Notes FSHT = enuresis alarm, overlearning after 14 dry nights, motivation + rewards, diary with fixed drinking and voiding times 
 PFMT = pelvic floor muscle training, 10 fast and 10 slow contractions daily at home 
 No useable data
Risk of bias
Bias Authors' judgement Support for judgement
Allocation concealment? Unclear risk D ‐ Not used

A = Alarm; CT = Cleanliness Training (changing the bed); DBT = Dry Bed Training (training night, CT, PP and W); FSHT = Full Spectrum Home Training (A + CT + Overlearning + Retention Control Training); No. = number; NS = Not Significant; Overlearning = after success in achieving dry nights, child gets extra drinks at bed‐time to increase volume in bladder at night, and training is continued until dry again; PP = Positive Practice (practising getting up and voiding repeatedly); RCT = Randomised controlled trial; Retention Control Training = increasing bladder capacity by progressively delaying voiding, may include pelvic floor muscle training by stream interruption; W = Waking (waking child to void, earlier on subsequent nights if dry);

Characteristics of excluded studies [ordered by study ID]

Study Reason for exclusion
Azrin 1973 Excluded because participants were adults, and no useable data provided. 
 RCT: Yes 
 Comparison group: Yes 
 Organic causes excluded: Yes 
 Systematic baseline measurement of wetting: Yes 
 Systematic outcome measure: Yes 
 Intervention: Alarms, dry bed training in adults with severe learning difficulties in a state hospital
Bollard 1977 RCT: no 
 Comparison group: yes 
 Systematic baseline: no 
 Organic causes excluded: yes 
 Systematic outcome measure: yes 
 Intervention: DBT with parents as trainers with and without alarm
Doleys 1977b Excluded because children moved from B to A, therefore data unreliable 
 RCT: CCT (stratified by baseline wetting frequency and sex, method of allocation not specified) 
 Comparison group: yes 
 Systematic baseline: yes 
 Organic causes excluded: yes 
 Intervention: Dry bed training (alarm, training night, PP, CT, rewards for dry nights) versus Retention control training (stop‐start training, progressive increase in bladder capapcity)
Griffiths 1982 RCT: no 
 Comparison group: no 
 Systematic baseline: yes 
 Organic causes excluded: no 
 Systematic outcome measure: no 
 Intervention: DBT in children
Hanson 1988 Excluded because population was young adults (age 13‐29) with learning difficulties in residential centre 
 RCT: Yes 
 Comparison group: Yes 
 Organic causes excluded: No 
 Systematic baseline measurement of wetting: Yes 
 Systematic outcome measures: Yes 
 Interventions: Alarms, DBT, yoked awakening, rewards
Hunt 1989 RCT: no 
 Comparison group: no 
 Systematic baseline: yes 
 Organic causes excluded: yes 
 Systematic outcome measure: yes 
 Intervention: DBT
Kaplan 1988 RCT: no 
 Comparison group: yes 
 Organic causes excluded: yes 
 Systematic baseline measurement of wetting: no 
 Systematic outcome measures: yes 
 Interventions: Alarms, dry bed training, motivation
Nettelbeck 1979 RCT: no 
 Comparison group: yes 
 Systematic baseline: yes 
 Organic causes excluded: yes 
 Systematic outcome measure: yes 
 Intervention: DBT
Schulz 1978 RCT: no 
 Comparison group: yes 
 Systematic baseline: no 
 Organic causes excluded: yes 
 Systematic outcome measure: yes 
 Intervention: DBT, alarms
Smith 1979 Excluded because population had daytime wetting 
 RCT: yes (CCT) 
 Intervention: alarms, behaviour training (individual versus group)
van Son 1990 RCT: no 
 Comparison group: no 
 Intervention: DBT in 9 adults
Whelan 1990 Excluded because two separate RCTs were combined (effectively results presented for groups at different times, and no results from control groups) 
 RCT: yes 
 Comparison group: yes but no data provided 
 Systematic baseline: yes 
 Organic causes excluded: no 
 Systematic outcome measure: not by group allocation 
 Interventions: FSHT + alarm + (in second RCT) waking schedule

DBT = Dry Bed Training; FSHT = Full Spectrum Home Training

Contributions of authors

This review is based on work originally carried out at the NHS Centre for Reviews and Dissemination, University of York (see acknowledgements). CMAG used the data extracted by the York reviewers, added new trials and drafted the text. Duplicate data abstraction was provided by REP. All authors contributed to editing the text, and JHCE also provided clinical perspective and interpretation.

Sources of support

Internal sources

  • National Health Service Research and Development Programme, UK.

External sources

  • No sources of support supplied

Declarations of interest

JHCE has received reimbursement for attending a conference, fees for lecturing and a consultancy fee which was paid into a research fund from Ferring Pharmaceuticals, manufacturers of desmopressin. He is also an author of one of the included trials (Redsell 2003).

New search for studies and content updated (no change to conclusions)

References

References to studies included in this review

Azrin 1974 {published data only}

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