NCT07676149

Brief Summary

The purpose of this study is to evaluate the intra-observer and inter-observer reliability of the Kinovea video analysis software in measuring knee and hip angles during the sit-to-stand movement. Participants will perform sit-to-stand tasks while being video-recorded. The recorded movements will be analyzed using the Kinovea software to determine the consistency and reliability of joint angle measurements.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
35

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

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

First Submitted

Initial submission to the registry

June 24, 2026

Completed
5 days until next milestone

Study Start

First participant enrolled

June 29, 2026

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 30, 2026

Completed
20 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 20, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 20, 2026

Completed
Last Updated

June 30, 2026

Status Verified

June 1, 2026

Enrollment Period

21 days

First QC Date

June 24, 2026

Last Update Submit

June 24, 2026

Conditions

Keywords

KinoveaReliabilitySit-to-standVideo analysisJoint anglesInter-rater reliabilityIntra-rater reliabilityHip jointKnee joint

Outcome Measures

Primary Outcomes (2)

  • Hip Flexion

    Participants will perform a sit-to-stand task using a standard chair while lower extremity movements are recorded with a camera. The recorded videos will be transferred to the Kinovea software for the measurement of hip joint angles. To facilitate angle calculation, anatomical landmarks including the greater trochanter, the longitudinal axis of the trunk, and the midpoint of the thigh will be marked on the participant's clothing. Hip joint angles will then be analyzed using the angle measurement tool available in the software. Measurements will be performed independently by three physiotherapists at one-week intervals.

    At baseline (single video recording session)

  • Knee Flexion

    Participants will perform a sit-to-stand task using a standard chair while lower extremity movements are recorded with a camera. The recorded videos will be transferred to the Kinovea software for knee joint angle analysis. To calculate knee joint angles, anatomical landmarks including the greater trochanter, lateral femoral condyle, and lateral malleolus will be marked on the participant's clothing. Knee joint angles will then be analyzed using the angle measurement tool within the software. Measurements will be performed independently by three physiotherapists at one-week intervals.

    At baseline (single video recording session)

Study Arms (1)

Healthy Adults

The study consists of a single group. This group will comprise healthy individuals who meet the predefined inclusion and exclusion criteria.

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of volunteer students recruited from the Ankara Yildirim Beyazit University, Department of Physiotherapy and Rehabilitation at the Faculty of Health Sciences.

You may qualify if:

  • Be between the ages of 18 and 45
  • Have a body mass index (BMI) between 18 and 25 kg/m²
  • Be able to sit down and stand up independently
  • Be a volunteer

You may not qualify if:

  • Having previously undergone lower extremity and spinal surgery
  • Having a neurological, orthopedic, or vestibular condition that may affect balance and muscle strength
  • Having sustained a lower extremity and/or spinal injury within the last 6 months
  • Having spinal problems such as scoliosis or lumbar disc herniation
  • Having congenital orthopedic problems such as hemimelia, dysmelia, or leg length discrepancy
  • Being pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Yıldırım Beyazıt University

Ankara, Turkey (Türkiye)

Location

Central Study Contacts

Sevilay Seda BAŞ, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Asst. Prof.

Study Record Dates

First Submitted

June 24, 2026

First Posted

June 30, 2026

Study Start

June 29, 2026

Primary Completion

July 20, 2026

Study Completion

July 20, 2026

Last Updated

June 30, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

To protect participant privacy and because explicit consent for data sharing was not obtained.

Locations