Assessing Posture and ROM With PhysioMaster in Stroke Patients
Validity and Reliability of the PhysioMaster in Assessing Posture and Range of Motion in Patients With Stroke
1 other identifier
observational
60
1 country
1
Brief Summary
The smartphone application named PhysioMaster is an easy-to-use, accessible, and freely available application. Although it has been used in several previous studies, no validity or reliability study has yet been conducted in patients with stroke. Therefore, the aim of this study is to investigate the validity and reliability of the PhysioMaster smartphone application in patients with stroke. Accordingly, our hypotheses are as follows:
- H0: The PhysioMaster application is not a valid and reliable measurement tool for the assessment of posture and range of motion in patients with stroke.
- H1: The PhysioMaster application is a valid and reliable measurement tool for the assessment of posture and range of motion in patients with stroke. Participants will not take any intervention. Participants will be evaluated in terms of posture and range of motion by using PhysioMaster, Universal Goniometer and PostureScreen Mobile. During the first-day assessment, physiotherapists A and B will complete both the PhysioMaster application assessments and all other evaluations on the same patient without seeing each other's assessment scores. In order to evaluate the test-retest reliability of the application, physiotherapist A will repeat the assessments on Physiomaster on the same patient after 3 days.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jun 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 15, 2026
CompletedStudy Start
First participant enrolled
June 20, 2026
CompletedFirst Posted
Study publicly available on registry
July 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
July 8, 2026
July 1, 2026
2 months
June 15, 2026
July 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Posture Assessment with PhysioMaster
Posture will be measured by using the mobile phone application.
Day 1
PhysioMaster Range of Motion Assessment
Upper and lower extremity range of motion will be measured using a mobile phone application.
Day 1
Secondary Outcomes (2)
Range of Motion Assessment with Universal Goniometer
Day 1
Posture Assessment with PostureScreen
Day 1
Study Arms (1)
Patients with Stroke
Eligibility Criteria
Outpatient stroke patients from a rehabilitation clinic
You may qualify if:
- 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
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Beylikdüzü Fizik Tedavi ve Danışmanlık Merkezi
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Esra Çoban
Istinye University
- STUDY CHAIR
Pelin Arslan
Istinye University
- STUDY CHAIR
Sıla Yavuz
Istinye University
- STUDY CHAIR
Şevval Yılmazer
Istinye University
Central Study Contacts
Duru Delibalta
CONTACT
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 3 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Asst. Prof.
Study Record Dates
First Submitted
June 15, 2026
First Posted
July 8, 2026
Study Start
June 20, 2026
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
July 8, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will not share