Christensen 1981.
Methods | Quasi‐randomised controlled trial comparing 1 intervention group (a combination of articulation and oral myofunctional (tongue thrust) therapy) and 1 control group (articulation therapy only). (The date of the study was not reported.) | |
Participants | 10 children (6 boys and 4 girls) aged 5 years 8 months to 6 years 9 months. All participants had "normal hearing as measured by puretone screening tests, normal development as reported by parents, no other known physical or psychological abnormalities, no previous speech or tongue thrust services, willingness of the parents to cooperate and carry out daily home practice sessions, and white middle‐class home environment" (p 161). In addition, "all children...were observed by the investigator to have visually and acoustically distorted /s/ and /z/, 2 or more other dentally or interdentally produced tongue‐tip sounds (although acoustically correct) and interdental tongue positioning on swallows of all 3 swallowing media (liquid, solids and saliva)" (p 162) | |
Interventions | The 10 participants were randomly assigned to 1 of 2 groups Intervention group (n = 5)
Control group (n = 5)
At the start of the intervention, about 1.5 to 2.5 therapy sessions were devoted to articulation therapy targeting the placement of speech sounds /t/, /d/, /l/ and /n/ for all participants. As stated above, the frequency of therapy sessions was the same for both intervention and control groups. Total therapy time was 11 hours for each participant. All participants "were given weekly home assignments to be completed with the mother's help in brief, daily home practices" (p 162). "Articulation home assignments" and home assignments for oral myofunctional therapy were mentioned, but it was not clear whether the intervention group was given both home assignments and the control group was given only articulation home assignments (p 162) |
|
Outcomes | The following tests were used for pretreatment and post‐treatment assessments of articulation
Additional items were used for post‐treatment assessments of articulation
|
|
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | The method used to generate the random sequence was not described |
Allocation concealment (selection bias) | Unclear risk | The method used to conceal allocation was not described |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Blinding of participants and personnel was not possible |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Blinding of the outcome assessor was ensured ‐ "pre‐ and post‐treatment test responses were evaluated by two independent observers... Neither judge knew which children were receiving tongue‐thrust services" (p 162) |
Incomplete outcome data (attrition bias) All outcomes | Low risk | All participants completed the 22 therapy sessions |
Selective reporting (reporting bias) | Low risk | The study appears to be free of selective reporting bias |
Other bias | Low risk | The study appears to be free of other bias |