NCT07690982

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
0mo left

Started Jun 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress62%
Jun 2026Sep 2026

First Submitted

Initial submission to the registry

June 15, 2026

Completed
5 days until next milestone

Study Start

First participant enrolled

June 20, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

July 8, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Last Updated

July 8, 2026

Status Verified

July 1, 2026

Enrollment Period

2 months

First QC Date

June 15, 2026

Last Update Submit

July 7, 2026

Conditions

Keywords

ROMPostureAlignmentTele-assessmentSmartphone application

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

Age40 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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)

Location

MeSH Terms

Conditions

Stroke

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Study Officials

  • Esra Çoban

    Istinye University

    STUDY CHAIR
  • Pelin Arslan

    Istinye University

    STUDY CHAIR
  • Sıla Yavuz

    Istinye University

    STUDY CHAIR
  • Şevval Yılmazer

    Istinye University

    STUDY CHAIR

Central Study Contacts

Çiçek Günday, Asst. Prof

CONTACT

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

Locations