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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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07690982
Enrollment
60
Registered
2026-07-08
Start date
2026-07-13
Completion date
2026-09-26
Last updated
2026-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

ROM, Posture, Alignment, Tele-assessment, Smartphone application

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.

Detailed description

Participants will not take any intervention.

Interventions

None listed

Sponsors

Istinye University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
40 Years to 70 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Posture Assessment with PhysioMasterDay 1Posture will be measured by using the mobile phone application.
PhysioMaster Range of Motion AssessmentDay 1Upper and lower extremity range of motion will be measured using a mobile phone application.

Secondary

MeasureTime frameDescription
Range of Motion Assessment with Universal GoniometerDay 1Upper and lower extremity range of motion will be measured using a universal goniometer.
Posture Assessment with PostureScreenDay 1Posture will be measured by using the mobile phone application.

Countries

Turkey (Türkiye)

Contacts

CONTACTÇiçek Günday, Asst. Prof
cicek.gunday@istinye.edu.tr+90 850 283 60 00
CONTACTDuru Delibalta
STUDY_CHAIREsra Çoban

Istinye University

STUDY_CHAIRPelin Arslan

Istinye University

STUDY_CHAIRSıla Yavuz

Istinye University

STUDY_CHAIRŞevval Yılmazer

Istinye University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 12, 2026