Trial · NCT07893925
The Effects of Synchronous and Asynchronous Pilates Training Based on Telerehabilitation on Core Stabilization, Balance, Cognitive Functions, and Quality of Life in Individuals With Multiple Sclerosis: A Single-Blind Randomized Controlled Trial
NCT07893925, Not applicable, Recruiting, Yuzuncu Yil University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. The Effects of Synchronous and Asynchronous Pilates Training Based on Telerehabilitation on Core Stabilization, Balance, Cognitive Functions, and Quality of Life in Individuals With Multiple Sclerosis: A Single-Blind Randomized Controlled Trial. Trials, record NCT07893925. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07893925
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
The Effects of Synchronous and Asynchronous Pilates Training Based on Telerehabilitation on Core Stabilization, Balance, Cognitive Functions, and Quality of Life in Individuals With Multiple Sclerosis: A Single-Blind Randomized Controlled Trial
- NCT number
- NCT07893925
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 38 participants, estimated
- Lead sponsor
- Yuzuncu Yil University
- Conditions
- Multiple Sclerosis
- Interventions
- Synchronous Telerehabilitation-Based Pilates, Asynchronous Telerehabilitation-Based Pilates
- First posted
- 2026-10-26
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Trunk Flexor Endurance | Baseline and immediately after the 8-week intervention. | Trunk flexor endurance will be assessed by measuring how long participants can maintain a seated position with the trunk at 60 degrees of flexion, hips and knees at 90 degrees, arms crossed over the chest, and feet stabilized. The test ends when the position can no longer be maintained. Duration is recorded in seconds; longer durations indicate better endurance. |
| Primary | Change in Sit-Up Performance | Baseline and immediately after the 8-week intervention. | Participants will perform sit-ups from a supine position with knees flexed and feet stabilized by the physiotherapist. The number of successfully completed repetitions will be recorded. Higher repetition counts indicate better performance. |
| Primary | Change in Modified Push-Up Performance | Baseline and immediately after the 8-week intervention. | Participants will begin in a prone position with hands at shoulder level and elbows flexed alongside the trunk. They will extend their elbows to lift the head, shoulders, and trunk from the floor. The number of successfully completed repetitions will be recorded. Higher repetition counts indicate better performance. |
| Secondary | Change in Activities-Specific Balance Confidence Scale Score | Baseline and immediately after the 8-week intervention. | This 16-item self-report scale assesses confidence in maintaining balance during daily activities. Each item is rated from 0 to 100, and the total score is the mean of the item scores. Higher scores indicate greater balance confidence. |
| Secondary | Change in Mini-BESTest Score | Baseline and immediately after the 8-week intervention. | The Mini Balance Evaluation Systems Test assesses anticipatory postural adjustments, reactive postural control, sensory orientation, and dynamic gait. It includes 14 items scored from 0 to 2, giving a total score of 0-28. Higher scores indicate better balance. |
| Secondary | Change in Symbol Digit Modalities Test Score | Baseline and immediately after the 8-week intervention. | The Symbol Digit Modalities Test, administered as part of the BICAMS battery, assesses cognitive processing speed. The number of correct symbol-digit substitutions completed within 90 seconds is recorded. Higher scores indicate better performance. |
| Secondary | Change in California Verbal Learning Test Score | Baseline and immediately after the 8-week intervention. | The California Verbal Learning Test, administered as part of the BICAMS battery, assesses verbal learning and memory. Performance is measured by the total number of words correctly recalled across the initial five learning trials. Higher scores indicate better verbal learning. |
| Secondary | Change in Brief Visuospatial Memory Test-Revised Score | Baseline and immediately after the 8-week intervention. | The Brief Visuospatial Memory Test-Revised, administered as part of the BICAMS battery, assesses visuospatial learning and memory. Performance is measured by the total recall score across three learning trials. Higher scores indicate better visuospatial learning. |
| Secondary | Change in Preference-Based Multiple Sclerosis Index Score | Baseline and immediately after the 8-week intervention. | This patient-reported measure assesses health-related quality of life across walking, fatigue, mood, concentration, and roles and responsibilities. Responses are combined into a preference-based index score. Higher scores indicate better health-related quality of life. |
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.
Tests2
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 |
|---|---|---|
| Symbol Coding | Secondary outcome | ConductCognition |
| Verbal Learning | Secondary outcome | 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/NCT07893925
GET https://conductscience.org/api/trials/v1/NCT07893925/registered