The Effect of Orofacial Myofunctional Therapy With Autofeedback on Obstructive Sleep Apnea
NCT06079073, Not applicable, Completed, University Hospital, Akershus
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | The Effect of Orofacial Myofunctional Therapy With Autofeedback on Obstructive Sleep Apnea | ClinicalTrials.gov |
| NCT number | NCT06079073 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 106 participants, actual | ClinicalTrials.gov |
| Lead sponsor | University Hospital, Akershus | ClinicalTrials.gov |
| Conditions | Sleep Apnea, Obstructive | ClinicalTrials.gov |
| Interventions | Orofacial myofunctional therapy with autofeedback | ClinicalTrials.gov |
| First posted | 2023-10-12 | ClinicalTrials.gov |
| Last updated | 2025-04-01 | ClinicalTrials.gov |
Registered outcomes 16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Apnea hypopnea index reduction | 3 months | Measured by self-applied somnography. The index represents number of apneas or hypopneas per hour from 0/h. Higher values represents more severe disease. | ClinicalTrials.gov |
| Secondary | Change in the Epworth Sleepines scale | 3 months | The scale is a validated tool measuring sleepiness between 0-24. Higher values represent more sleepiness | ClinicalTrials.gov |
| Secondary | Orofacial myofunctional therapy adherence | 3 months | Measured by application registration between 1-3 per day. Three exercises per day is the maximum score | ClinicalTrials.gov |
| Secondary | Change in desaturation severity parameter measured by medical device | 3 months | Measured by photoplethysmography obtained by self-applied somnography. More severity represents more disease. | ClinicalTrials.gov |
| Secondary | Change in desaturation duration measured by medical device | 3 months | Measured by photoplethysmography obtained by self-applied somnography. Longer duration represents more disease. | ClinicalTrials.gov |
| Secondary | Change in objective sleep quality | 3 months | Measured by self-applied somnography. Sleep quality is the ratio between total sleep time and time in bed. A higher ratio is better. | ClinicalTrials.gov |
| Secondary | Change in desaturation severity parameter measured by wearable | 3 months | Measured by photoplethytsmography obtained by Withings Scan Watch. More severity represents more disease. | ClinicalTrials.gov |
| Secondary | Change in desaturation duration measured by wearable | 3 months | Measured by photoplethytsmography obtained by Withings Scan Watch. Longer duration represents more disease. | ClinicalTrials.gov |
| Secondary | Change in stroop test | 3 months | Measured by Flexibility game in application. More correct answers is better | ClinicalTrials.gov |
| Secondary | Change in reaction test | 3 months | Measured by reaction game in application. Shorter reaction time is better | ClinicalTrials.gov |
| Secondary | Change in memory test | 3 months | Measured by memory game in application. Longer sequences memorized is better | ClinicalTrials.gov |
| Secondary | Change in perception test | 3 months | Measured by perception game in application. More correct answers is better. | ClinicalTrials.gov |
| Secondary | Change general health status | 3 months | Measured by a visual analogue scale in the BEAMER questionnaire, two visio analogue scales on general health and 3 items on acceptance and control scored 1-6 respectively. | ClinicalTrials.gov |
| Secondary | Changes in the Orofacial Myofunctional Evaluation with Scores | 3 months | Measured by scorer blinded for randomization. Range 37-103. A lower score represents more dysfunction. | ClinicalTrials.gov |
| Secondary | Changes in tongue strength | 3 months | Objective strength measured by the Iowa Oral Pressure Inventory. A higher score represents more strenght. | ClinicalTrials.gov |
| Secondary | Changes in tongue endurance | 3 months | Objective endurance measured by the Iowa Oral Pressure Inventory. A higher score represents more endurance. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 2
The papers the trial lists on ClinicalTrials.gov.
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)