Cross Cultural Adaptation, Validity and Reliability Test of the Arabic Version of the Outpatient Physical Therapy Improvement in Movement Assessment Log

NCT06282744 | Not Yet Recruiting

• 1 other identifier: OPTIMAL Arabic version
• Study Type: observational
• Target: 880
• Locations: 0 countries
• Sites: N/A

Brief Summary

Purpose of the study: To translate, culturally adapt, and to test the validity and reliability of the Outpatient Physical Therapy Improvement in Movement Assessment Log in Arabic speaking language.

Conditions

Physical Performance; Outpatients

Keywords

Questionnaire; OPTIMAL; Validity testing; Arabic version; Psychometric properties; Reliability Testing

Outcome Measures

Primary Outcomes (1)

• validity and reliability of the Egyptian Arabic language version of Outpatient Physical Therapy Improvement Movement Assessment Log on physical therapy outpatients.

  to test if the Arabic version of this log is valid for usage among Egyptian People. Test improvement in different movements.

  Up to 24 weeks

Interventions

Outpatient physical therapy improvement in movement assessment log OTHER

The Outpatient Physical Therapy Improvement in Movement Assessment Log (OPTIMAL) is an instrument that measures difficulty and self-confidence in performing 22 movements that a patient needs to accomplish in order to do various functional activities.

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Egyptian adults who took at least a month of physiotherapy sessions.

You may qualify if:

• Participants are adult outpatients who took at least a month of physiotherapy sessions.
• Both genders will be included.
• At least 18 years of age.
• Participants must be conscious and ambulant.
• Participants able to read, write Arabic as a mother tongue and understand the instructions, questions in the questionnaire.

You may not qualify if:

• Participants having the following conditions will be excluded from the study:
• Patients who are not able to provide informed consent.
• Patients who are unable to complete the OPTIMAL instrument.
• Patients who have a severe cognitive impairment.
• Patients who are not receiving physical therapy.
• Patients who are not Arabic-speaking.
• Patients who have a history of malingering

Sponsors & Collaborators

• Cairo University: lead

Central Study Contacts

Eman Hamdy Abdeltwab Hussien

CONTACT

+201066718447; emanhamdy291194@gmail.com

Nabil Mahmoud

CONTACT

+01200133613; nabil.mahmoud@cu.edu.eg

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Dr Eman Hamdy

Study Record Dates

• First Submitted: January 14, 2024
• First Posted: February 28, 2024
• Study Start: March 1, 2024
• Primary Completion: March 1, 2024
• Study Completion: April 1, 2024
• Last Updated: February 28, 2024

Record last verified: 2024-02