Translation & Psychometric Properties of the Fatigue Severity Scale in

Status Recruiting

Clinical Trial Summary

The study will employ a Cross-Sectional Validation Study design. The study will be conducted at the Department of Physical Therapy, University of Lahore Teaching Hospital, located on Defence Road, Lahore. The anticipated duration of the study will be 09 months, commencing after the approval of the synopsis. The sample size will be determined following the Kline Method, resulting in a total of 90 participants. A Purposive Sampling Technique will be utilized to select the study participants.

Clinical Trial Description

Study Type: Cross-Sectional Validation Study Location: Department of Physical Therapy, University of Lahore Teaching Hospital, Defence Road, Lahore Duration: 06 months (post-synopsis approval) Sample Size: 90 participants Sampling Technique: Purposive Sampling Consent and Ethics: Participants will provide written informed consent. Ethics approval will be obtained from the University of Lahore Ethics Committee. Translation of FSS: The Fatigue Severity Scale (FSS) will be translated into Urdu for data collection. Two independent bilingual translators will create reports on translation difficulties and rationale. These reports will inform a consensus meeting to develop a unified Urdu version, with comments documented. The unified version will be backtranslated into English by native English-speaking translators unaware of the questionnaire's concept. Expert Committee: An expert committee comprising physical therapists, linguists, and a methodologist will review both language versions. The goal is to ensure semantic, idiomatic, experiential, and conceptual equivalence and reach consensus on the final Urdu version of the FSS. Patient Involvement: The final Urdu FSS version will be administered to 20 fibromyalgia patients. These patients will also be interviewed to assess their understanding of questionnaire items. Participants will receive additional information about fibromyalgia to prevent confusion. Data Collection: Data will be collected from 100 fibromyalgia patients using the final Urdu FSS version. A retest will be conducted after 48 hours. Additional Assessment: All 90 participants will complete the Multidimensional Fatigue Inventory (MFI). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06031207
Study type	Observational
Source	University of Lahore
Contact	Ashfaq Ahmad, PhD
Phone	03009449192
Email	dean@ahs.uol.edu.pk
Status	Recruiting
Phase
Start date	September 1, 2023
Completion date	January 2024

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See also
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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Translation and Psychometric Properties of the Fatigue Severity Scale in Patients With Fibromyalgia

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms