Trial · NCT07879859
Feasibility and Acceptability of a 6-Week Myofunctional and Physical Activity Program for University Students With Excessive Daytime Sleepiness
NCT07879859, Not applicable, Completed, Kuwait University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Feasibility and Acceptability of a 6-Week Myofunctional and Physical Activity Program for University Students With Excessive Daytime Sleepiness. Trials, record NCT07879859. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07879859
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Feasibility and Acceptability of a 6-Week Myofunctional and Physical Activity Program for University Students With Excessive Daytime Sleepiness
- NCT number
- NCT07879859
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 14 participants, actual
- Lead sponsor
- Kuwait University
- Conditions
- Excessive Daytime Sleepiness, Disorders of Excessive Somnolence
- Interventions
- MYOPAP Program
- First posted
- 2026-10-19
- Last updated
- 2026-10-19
Source ClinicalTrials.gov
Registered outcomes6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Retention Rate | Baseline to week 6 | Proportion of enrolled participants who completed the 6- week program. |
| Primary | Adherence to the exercise program | week 1 to 6 | Proportion of participants who completed the myofunctional exercises on at least 3 days per week, monitored using daily electronic polls. |
| Primary | Intervention acceptability | Week 6 | Proportion of participants who somewhat or completely agreed with each item of a 9-item post-intervention acceptability questionnaire (5-point Likert scale scored 0-4, from completely disagree to completely agree). |
| Primary | Number of participants with Adverse Events | Weeks 1 to 6 | Participants-reported adverse effects related to the intervention, recorded at weekly follow-up sessions. |
| Primary | Recruitment Rate | Recruitment period (3 weeks) | Proportion of eligible students (ESS\>10) contacted who consented and enrolled in the study. Reported descriptively because of the sequential, capped recruitment design. |
| Secondary | Change in Daytime Sleepiness | Baseline and week 6 | Change in ESS total score from baseline to week 6 (exploratory). |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
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.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07879859
GET https://conductscience.org/api/trials/v1/NCT07879859/registered