Turkish Version of the Chalder Fatigue Scale: An Investigation of Its Psychometric Properties in Healthy Young Adults

Sponsor
Hacettepe University (Other)
Overall Status
Completed
CT.gov ID
NCT03969667
Collaborator
(none)
353
1
8.8
40.1

Study Details

Study Description

Brief Summary

The aim of this study was to adapt the Chalder Fatigue Scale to Turkish and to examine its psychometric properties in young adults. Within the scope of the study, firstly the Turkish version of the scale will be developed and then its reliability and validity will be examined in healthy young adults in Turkey.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Fatigue is a subjective experience that can affect all individuals. It is a protective symptom against physical or psychological stress for healthy individuals. However, it can negatively affect the performance of individuals in activities of daily living. In the clinic, fatigue is assessed by self-reported scales. Different fatigue scales have some advantages and disadvantages compared to each other. Moreover, it is stated that only one scale cannot fully measure the fatigue of individuals in different health status, therefore different scales have been developed.Chalder Fatigue Scale (CFS) is an easy-to-understand, short, fast and useful fatigue scale that evaluates fatigue with two dimensions (physical and mental) and enable individuals to express perceived fatigue clearly. Psychometric properties of CFS have been investigated in general population and different disease groups but not in only healthy young adults.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    353 participants
    Observational Model:
    Other
    Time Perspective:
    Cross-Sectional
    Official Title:
    Turkish Version of the Chalder Fatigue Scale: An Investigation of Its Psychometric Properties in Healthy Young Adults
    Actual Study Start Date :
    May 15, 2019
    Actual Primary Completion Date :
    Jan 10, 2020
    Actual Study Completion Date :
    Feb 7, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    healthy young adults

    healthy young adults

    Outcome Measures

    Primary Outcome Measures

    1. The Turkish Version of the Chalder Fatigue Scale [About 2-3 minutes]

      The Chalder Fatigue Scale has a 7-item physical fatigue subscale and 4 items of mental fatigue subscale. The scale evaluates the severity of physical and mental fatigue over the last month. Each item is scored 0-3 (0=less than usual, 3=much more than usual), yielding a total between 0 and 33.

    2. The Turkish Version of the Checklist Individual Strength Fatigue Scale [About 3-4 minutes]

      The scale evaluates fatigue over the past two weeks.The questionnaire consists of 20 items with a 7-point Likert scale scoring. A total score is derived by summation of the item scores (20-140). There are four subscales; Fatigue Severity, measuring the subjective experience of fatigue (8 items); Concentration, measuring concentration problems (5 items); Motivation, measuring reduced motivation (4 items) and Activity, measuring the reduction of activities (3 items).

    Secondary Outcome Measures

    1. Visual Analog Scale to Evaluate Physical and Mental Fatigue [About 1 minutes]

      Self reported physical and mental fatigue severity over the last month. It is scored 0=no fatigue; 10= tired as bad as can be

    2. The Turkish Version of the Pittsburgh Sleep Quality Index [About 2-3 minutes]

      The scale assesses sleep quality over a 1-month period. The questionnaire consists of 19 self-rated questions and 5 questions that should be answered by roommates. The latter questions are used only for clinical information. The 19 questions are categorized into 7 components, graded on a score that ranges from 0 to 3. The scale's components are as follows: subjective sleep quality (C1), sleep latency (C2), sleep duration (C3), habitual sleep efficiency (C4), sleep disturbances (C5), use of sleeping medication (C6) and daytime dysfunction (C7). The sum of scores for these 7 components yields one global score, which ranges from 0 to 21, where the highest score indicates worst sleep quality.

    3. The Turkish Version of the Beck Depression Inventory [About 4-5 minutes]

      It is a 21-item self-report questionnaire for assessing the severity of depressive symptoms over past week; the items comprise four ordinal categories (from 0 through 3). Absence (or "as usual") of depressive symptom in each item is scored as "0" and presence of symptom is scored between 1 and 3, with the higher score indicating more intense symptom severity. The possible total score ranges from 0 to 63.

    4. The Turkish Version of the Nottingham Health Profile [About 4-5 minutes]

      The scale measures subjective health status using 38 items that assess 6 subscales (physical mobility, pain, energy level, sleep, emotional reaction and social isolation); each question answered by (yes) or (no) with each question assigned a weighted value. Scores for each section can range from 0 "no problems" to 100 "all problems listed are present" where the sum of all weighted values in a given subscale adds up to 100.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years to 40 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    The inclusion criteria for participants are: to be aged between 20 and 40 years old, volunteer to participate the study, able to read and speak Turkish.

    Exclusion criteria are determined as individuals with known acute or chronic health conditions and illnesses and who had surgery in the past 6 months.

    Further exclusion criteria are to take over-the-counter medication or food supplement, have abnormal body mass index (BMI) (lower 17 kg/m2 or higher 30 kg/m2), self reported depression as indicated by a score of > 21 on the Beck Depression Scale (BDS), pain as indicated by a score of > 0 on pain subscale of Nottingham Health Profile (NHP). Additionally, female participants were excluded if they use oral contraceptives, experience premenstrual syndrome or were pregnant within the last one year period.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hacettepe University Faculty of Health Sciences Department of Physiotherapy and Rehabilitation Ankara Altındag Turkey 06230

    Sponsors and Collaborators

    • Hacettepe University

    Investigators

    • Principal Investigator: Cigdem Ayhan, Assoc. Prof., Hacettepe University
    • Study Chair: Ridvan M Adin, R. A., Hacettepe University
    • Study Chair: Ali N Ceren, R. A., Hacettepe University
    • Study Chair: Ayla Fil Balkan, Asst. Prof., Hacettepe University
    • Study Chair: Yeliz Salci, Asst. Prof., Hacettepe University
    • Study Chair: Kadriye Armutlu, Prof., Hacettepe University

    Study Documents (Full-Text)

    More Information

    Publications

    Responsible Party:
    Cigdem Ayhan, associate doctor, Hacettepe University
    ClinicalTrials.gov Identifier:
    NCT03969667
    Other Study ID Numbers:
    • GO 19/512
    First Posted:
    May 31, 2019
    Last Update Posted:
    May 26, 2020
    Last Verified:
    May 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Cigdem Ayhan, associate doctor, Hacettepe University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 26, 2020