Trial · NCT07910981
Effects of a Multidisciplinary Intervention on Muscle Strength, Posture, and Balance in Older Adults After an Earthquake
NCT07910981, Not applicable, Completed, Kahramanmaras Sutcu Imam University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of a Multidisciplinary Intervention on Muscle Strength, Posture, and Balance in Older Adults After an Earthquake. Trials, record NCT07910981. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07910981
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of a Multidisciplinary Intervention on Muscle Strength, Posture, and Balance in Older Adults After an Earthquake
- NCT number
- NCT07910981
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 60 participants, actual
- Lead sponsor
- Kahramanmaras Sutcu Imam University
- Conditions
- Muscle Weakness, Postural Balance, Physical Functional Performance, Frail Elderly
- Interventions
- Multimodal Intervention
- First posted
- 2026-11-02
- Last updated
- 2026-11-02
Source ClinicalTrials.gov
Registered outcomes7
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Upper and Lower Extremity Muscle Strength | Baseline and Week 12 | Isometric muscle strength of selected upper- and lower-extremity muscle groups was assessed using the KFORCE KINVENT digital muscle strength measurement device. Measurements were performed bilaterally to evaluate changes in muscle strength following the 12-week intervention. |
| Primary | Change in Postural Alignment | Baseline and Week 12 | Postural alignment was assessed using the PostureScreen mobile application. Frontal and lateral photographs were obtained to identify postural deviations and evaluate changes in postural alignment following the intervention. |
| Primary | Change in Postural Sway and Balance | Baseline and Week 12 | Postural sway was assessed using the Gyko system. The assessment included sway length, sway area, sway progression rate, and sway frequency to evaluate postural stability and balance changes following the 12-week intervention. |
| Secondary | Change in Handgrip Strengt | Baseline and Week 12 | Handgrip strength was assessed using a Jamar hand dynamometer. Measurements were performed to evaluate changes in handgrip strength between baseline and the end of the 12-week intervention. |
| Secondary | Change in Pinch Strength | Baseline and Week 12 | Pinch strength was assessed using a mechanical pinch dynamometer (Baseline Pinch Gauge). Measurements were performed to evaluate changes in pinch strength following the intervention. |
| Secondary | Change in Functional Mobility and Dynamic Balance | Baseline and Week 12 | Functional mobility and dynamic balance were assessed using the Timed Up and Go Test (TUG). The time required to stand from a chair, walk three meters, turn, return, and sit down was recorded in seconds. Lower completion times indicate better functional mobility. |
| Secondary | Change in Lower Extremity Physical Performance | Baseline and Week 12 | Lower-extremity physical performance was assessed using the Short Physical Performance Battery (SPPB), consisting of standing balance, a four-meter walking test, and a chair-rise test. Total scores range from 0 to 12, with higher scores indicating better physical performance. |
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/NCT07910981
GET https://conductscience.org/api/trials/v1/NCT07910981/registered