Trial · NCT05416398
Effects of High-intensity Interval Training and Aerobic Exercise on Obstructive Sleep Apnea.
NCT05416398, Not applicable, Unknown, Inonu University
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Effects of High-intensity Interval Training and Aerobic Exercise on Obstructive Sleep Apnea. Trials, record NCT05416398. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05416398
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of High-intensity Interval Training and Aerobic Exercise on Obstructive Sleep Apnea.
- NCT number
- NCT05416398
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 33 participants, estimated
- Lead sponsor
- Inonu University
- Conditions
- Respiratory Function Loss, Exercise Capacity, Fatigue, Selective Attention, Physical Parameters
- Interventions
- Aerobic Exercise, High Intensity Interval Training
- First posted
- 2022-06-13
- Last updated
- 2022-06-13
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Pulmonary Function Tests | 8 week | Forced expiratory volume in 1 second (FEV1), forced vital capacity (FVC) and ratios will be used in statistical analysis.(FEV1/FVC) |
| Primary | Exercise Capacity | 8 week | Exercise capacity will be evaluated with a 6-minute walk test. Evaluates the integrated responses of all systems involved during exercise, including the pulmonary and cardiovascular systems, blood, neuromuscular system, and muscle metabolism. |
| Secondary | Fatigue | 8 week | It will be evaluated with the Fatigue Severity Scale. FSS is the most commonly used scale among the one-dimensional scales developed to assess fatigue. |
| Secondary | Selective Attention | 8 week | The Stroop Test will be used to evaluate selective attention. |
| Secondary | Disease-Specific quality of life | 8 week | Disease-Specific quality of life will be evaluated with Functional Outcomes of Sleep Questionnaire, FOSQ,tr). |
| Secondary | General Health-Related Quality of Life | 8 week | Overall health-related quality of life will be assessed with the Nottingham Health Profile. |
| Secondary | Daytime Sleepiness | 8 week | Epworth Sleepiness Scale will be used to measure the general sleepiness of the patients during the day. |
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.
Papers4
The papers the trial lists on ClinicalTrials.gov.
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.
Tests1
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 |
|---|---|
| Stroop Color-Word Test | Secondary outcome |
Source ConductCognition
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/NCT05416398
GET https://conductscience.org/api/trials/v1/NCT05416398/registered