See if PhysioMaster can accurately measure posture and range of motion in stroke patients
Official title: Validity and Reliability of the PhysioMaster in Assessing Posture and Range of Motion in Patients With Stroke
Run by Istinye University · NCT07690982 · Data updated 2026-11-12
This study tests whether the PhysioMaster smartphone app can accurately measure posture and joint movement in adults who had a stroke.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 40 Years to 70 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Istinye University Academic / other |
| Locations | 1 site (Istanbul) |
| Status | Recruiting |
| Started | July 13, 2026 |
| Main results expected | September 26, 2026 |
| Study ends | September 26, 2026 |
| Registry record updated | August 11, 2026 |
| Trial ID | NCT07690982 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 40–70 with a stroke who are at least six months post-event, able to stand independently for 1 minute, and able to follow instructions.
✕Probably not a fit
Patients with non-stroke neurological conditions, recent orthopedic surgery, or higher spasticity may not benefit from this tool in the current validation context.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study evaluates the validity and reliability of the PhysioMaster smartphone app for measuring posture and range of motion in stroke patients. Participants will be assessed using PhysioMaster, a universal goniometer, and PostureScreen Mobile without receiving any intervention. Therapists will perform assessments on the first day to compare measurements across devices. The study focuses on adults aged 40 to 70 who are at least six months post-stroke and meet specific functional criteria. No active treatment is provided during participation, and results will inform whether PhysioMaster can be a trustworthy tool for remote or in-clinic posture and ROM assessment in stroke care.
Why it matters
Potential benefit: If successful, patients could benefit from a convenient, smartphone-based option for monitoring posture and range of motion during stroke recovery.
How similar studies have gone: Some prior studies have used mobile and camera-based assessments, but formal validity/reliability data in stroke populations are limited, making this validation novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Presence of hemiplegia caused solely by stroke * Being older than 40 years and younger than 70 years of age * At least 6 months have passed since the stroke * Ability to maintain independent standing for at least 1 minute * Being at stage 4 or higher according to the Brunnstrom stages of stroke recovery * Ability to understand and follow instructions * Voluntary agreement to participate in the study Exclusion Criteria: * Presence of any neurological diagnosis other than stroke * History of orthopedic surgery within the last 6 months * Presence of concomitant orthopedic trauma * Presence of spasticity graded 3 or higher according to the Modified Ashworth Scale (MAS)
Where it's running
-
Beylikdüzü Fizik Tedavi ve Danışmanlık Merkezi
Istanbul, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Çiçek Günday, Asst. Prof
- Email: cicek.gunday@istinye.edu.tr
- Phone: +90 850 283 60 00
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.