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editorial
. 2002 Dec 7;325(7376):1312–1313. doi: 10.1136/bmj.325.7376.1312

Sensory stimulation in dementia

An effective option for managing behavioural problems

Alistair Burns 1,2,3,4, Jane Byrne 1,2,3,4, Clive Ballard 1,2,3,4, Clive Holmes 1,2,3,4
PMCID: PMC1124787  PMID: 12468458

Most older people with dementia at some point in their illness develop psychiatric symptoms or behavioural disturbances such as agitation, aggression, depression, delusions, wandering, sleep disturbance, and hallucinations. Collectively, these are termed behavioural and psychological symptoms of dementia.1 They are frightening for patients and their carers; constitute a major management problem for psychiatrists, general practitioners, and geriatricians; and act as a trigger for admission to institutional care. After excluding treatable causes such as concurrent infections, non-pharmacological approaches such as behavioural management are the recommended first line intervention.2

In practice, however, drugs such as neuroleptics and other sedatives are often prescribed in an attempt to control what can be an alarming situation. Although neuroleptics have modest term efficacy in the short term,3 they are associated with side effects such as sedation, extrapyramidal signs, falls, a detrimental impact on quality of life,4 and, possibly, accelerated cognitive decline.5 These side effects are most pronounced in people with severe dementia, exactly the group who have most behavioural and psychological symptoms and for whom no evidence is available from placebo controlled trials of neuroleptics or other psychotropic agents. A wide range of alternative approaches has been tried, including multisensory interventions such as snoozelan (involving fibreoptic lights and touch) but reports have essentially been qualitative and based on small numbers of patients. Two exceptions are aromatherapy and bright light treatment, which have emerged as promising treatments.

Aromatherapy has a long history and is the fastest growing of all complementary treatments. Three placebo controlled trials have been completed in the last year, and each has reported a significant beneficial effect on agitation compared with placebo, with almost complete compliance and no side effects (table). In addition, as opposed to neuroleptics, which seem to be associated with a detrimental impact on wellbeing, quality of life significantly improved with aromatherapy.8

Lemon balm (Melissa officinalis) or lavender oil (Lavendula officinalis) are the two main agents used and are delivered by either inhalation or skin application.68 Almost all participants in the studies completed the course of treatment. This emphasises the excellent tolerability of aromatherapy, which is in contrast to many of the pharmacological treatments in this group of patients—it is common for 30% or more of the participants to be unable to complete a trial. Explanations for the efficacy of aromatherapy range from subjective psychological to direct biological action. In the studies cited no extended period of massage was used, and a direct chemical effect seems therefore likely.6,8 Essential oils contain many terpenes, which are rapidly absorbed through the lungs and cross the blood-brain barrier. In addition, many possess cholinergic activity or act on γ aminobutyric acid receptors.12,13

Bright light is effective in the treatment of seasonal affective disorder.14 The technique involves sitting in front of a light box with the entire visual angle subtended by the light source—the amount of light is important (up to 10 000 lux compared with average office light, which is up to 300 lux). Three controlled trials have been published in the past three years that investigate the effect of bright light on sleep disturbance and behavioural disorders in dementia (table).911 Some benefits were reported for restlessness, but a particular beneficial effect has been found for sleep disturbances. These results are promising.

People with dementia are among the most vulnerable in our society. Symptoms often need to be treated expediently, and drugs, although moderately effective, can be hazardous. Aromatherapy and bright light treatment seem to be safe and effective and may have an important role in managing behavioural problems in people with dementia.

Table.

Aromatherapy and bright light treatment as interventions for behavioural and psychological symptoms of dementia

Study
Intervention and delivery method
Design
Patient group
Outcome
Other key points
Aromatherapy
Holmes et al6 2% Lavender oil via aromatherapy stream daily Double blind placebo controlled crossover (alternate days) for 10 days Severe dementia in NHS continuing care (n=15) Significant improvement in Philadelphia agitation scale (P=0.02), with 60% of patients having some benefit No adverse events
Compliance: 100%
Smallwood et al7 Twice weekly Two week single blind randomised controlled trial. Aromatherapy+massage v aromatherapy+conversation v massage alone Inpatients with severe dementia (n=21) Significant improvement (P<0.056) in motor behaviour (34% reduction with aromatherapy +massage)
Ballard et al8 Melissa oil (10% by weight combined with base lotion) via cream applied to hands twice daily (200 mg oil) Double blind placebo controlled trial. Melissa oil v sunflower oil Severe dementia in NHS continuing care (n=72) Significant (P<0.0001) improvement in Cohen Mansfield agitation inventory (median improvement of 22 points after active treatment) No major adverse effects. 97% of people assigned to active treatment completed the trial
Bright light treatment
Haffmanns et al9 Bright light 30 +/–morning (2.5 mg) melatonin or placebo Double blind placebo controlled crossover trial (n=10; 6 completed) DSM-IV dementia with motor restless behaviour Treatment reduced motor restlessness
Lyketsos et al10 1 hour bright light, morning Randomised controlled crossover trial (n=15; 8 completed) Dementia agitation Treatment increased total sleep time, no change in behaviour
Graf et al11 Evening bright light v dim light therapy Randomised bright light or dim light therapy (n=23) Dementia Treatment increased mini-mental state examination scores and led to a phase shift in body temperature rhythm

Footnotes

Competing interests: AB, CB, and JB have received honorariums, consultancy fees, and research grants from Janssen and Astra Zeneca, both of which manufacture products that are used in the management of behavioural disturbances in people with dementia. AB is editor of the International Journal of Geriatric Psychiatry, which publishes peer reviewed academic papers in old age psychiatry and occasionally publishes supplements sponsored by pharmaceutical companies.

References

  • 1.Finkel SI, Burns A, Cohen G. Behavioural and psychological symptoms of dementia: a clinical and research update. Int Psychogeriatr. 2000;12(s1):13–18. [Google Scholar]
  • 2.Herrmann N. Recommendations for the management of behavioral and psychological symptoms of dementia. Can J Neurol Sci. 2001;28 suppl 1:s96–107. doi: 10.1017/s0317167100001268. [DOI] [PubMed] [Google Scholar]
  • 3.Ballard CG, O'Brien J. Pharmacological treatment of behavioural and psychological signs in Alzheimer's disease: how good is the evidence for current pharmacological treatments? BMJ. 1999;319:138–139. doi: 10.1136/bmj.319.7203.138. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Ballard CG, O'Brien J, James I, Mynt P, Lana M, Potkins D. Quality of life for people with dementia living in nursing home and residential care. Int Psychogeriatr. 2001;13:93–106. doi: 10.1017/s1041610201007499. [DOI] [PubMed] [Google Scholar]
  • 5.McShane R, Keene J, Gedling K, Fairburn C, Jacoby R, Hope T. Do neuroleptic drugs hasten cognitive decline in dementia? Prospective study with necropsy follow up. BMJ. 1997;314:266–270. doi: 10.1136/bmj.314.7076.266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Holmes C, Hopkins V, Hensford C, MacLaughlin V, Wilkinson D, Rosenvinge H. Lavender oil as a treatment for agitated behaviour in severe dementia: a placebo controlled study. Int J Geriatr Psychiatry. 2002;17:305–308. doi: 10.1002/gps.593. [DOI] [PubMed] [Google Scholar]
  • 7.Smallwood J, Brown R, Coulter F, Irvine E, Copland C. Aromatherapy and behaviour disturbances in dementia: a randomized controlled trial. Int J Geriatr Psychiatry. 2001;16:1010–1013. doi: 10.1002/gps.473. [DOI] [PubMed] [Google Scholar]
  • 8.Ballard CG, O'Brien J, Reichelt K, Perry E. Aromatherapy as a safe and effective treatment for the management of agitation in severe dementia: the results of a double blind, placebo controlled trial. J Clin Psychiatr. 2002;63:553–558. doi: 10.4088/jcp.v63n0703. [DOI] [PubMed] [Google Scholar]
  • 9.Haffmanns PM, Sival RC, Lucius SA, Cats Q, van Gelder L. Bright light therapy and melatonin in motor restless behaviour in dementia: a placebo-controlled study. Int J Geriatr Psych. 2001;16:106–110. doi: 10.1002/1099-1166(200101)16:1<106::aid-gps288>3.0.co;2-9. [DOI] [PubMed] [Google Scholar]
  • 10.Lyketsos C, Veiel LL, Baker A, Steele C. A randomised controlled trial of bright light therapy for agitated behaviours in dementia patients residing in long-term care. Int J Geriatr Psych. 1999;14:520–525. [PubMed] [Google Scholar]
  • 11.Graf A, Wallner C, Schubert V. The effects of light therapy on mini-mental state examination scores in demented patients. Biol Psychiatry. 2001;50:725–727. doi: 10.1016/s0006-3223(01)01178-7. [DOI] [PubMed] [Google Scholar]
  • 12.Perry N. Cholinergic transmitter activities in European herbs: potential in dementia therapy. Int J Geriatr Psych. 1996;11:1063–1069. [Google Scholar]
  • 13.Ozoe Y, Akamatsu M, Higata T. Picrodendrin and related terpenoid antagonists reveal structural differences between ionotropic GABA receptors of mammals and insects. Bioorg Med Chem. 1998;6:481–492. doi: 10.1016/s0968-0896(98)00012-1. [DOI] [PubMed] [Google Scholar]
  • 14.Potkin SG, Zetin M, Stamenkovic V, Kripke D, Bunney WE., Jr Seasonal affective disorder: prevalence varies with latitude and climate. Clin Neuropharmacol. 1986;9 suppl 1:181–183. [PubMed] [Google Scholar]

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