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Completed

NCT Number: NCT06758999

Validity and Reliability of the Turkish Form of the OPTIMAL

The primary aim of the study was to determine the reliability and validity of the Turkish version of the questionnaire named "The Outpatient Physical Therapy Improvement in Movement Assessment Log". The secondary aim of the study was to measure the physical activity and mobility of outpatients receiving physical therapy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Kirsehir Ahi Evran University

Kırşehir, Merkez, 40100, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being 18 years of age or older
  • Receiving outpatient physical therapy
  • Volunteering to participate in the study
  • Knowing how to read and write

Exclusion criteria

  • Having a cognitive problem that prevents you from completing the survey independently.

Treatment and study plan

Primary outcomes

  1. The Outpatient Physical Therapy Improvement in Movement Assessment Log

    Time frame: 20 weeks

Secondary outcomes

  1. International Physical Activity Questionnaire

    Time frame: 20 weeks

Sponsors and collaborators

Lead sponsor

Kirsehir Ahi Evran Universitesi

Other

Registry information

Official study title

Validity and Reliability of the Turkish Form of the Outpatient Physical Therapy Improvement in Movement Assessment Log

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Jan 6, 2025
Registry last updated
Feb 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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