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Turkish Version of the BARSE (BARSE-Turkish)

26 ottobre 2026 aggiornato da: Irem Hüzmeli, Mustafa Kemal University

Validity and Reliability Study of the Barrier Specific Self-Efficacy Scale in Turkish

Background Physical inactivity is known to rank fourth among modifiable mortality risk factors globally and plays a central role in the etiology of noncommunicable diseases. In the context of physical activity, self-efficacy is a multidimensional construct, primarily divided into task self-efficacy and barrier self-efficacy. While task self-efficacy is crucial for initiating physical activity, barrier self-efficacy-the individual's belief in their capability to maintain exercise in the face of various physical, social, or psychological obstacles-is essential for long-term adherence. The Barrier-Specific Self-Efficacy Scale (BARSE), developed by McAuley et al., is specifically designed to measure this barrier self-efficacy dimension. A comprehensive literature review revealed no published Turkish validity and reliability study of the BARSE. Signed permission has been obtained from the original author to conduct this cultural adaptation.

Objectives The primary aim of this study is to investigate the validity and reliability of the Turkish version of the BARSE among healthy young adults, thereby contributing a standardized, culturally adapted instrument to the scientific community.

Study Design and Procedures This methodological study will conduct at the Faculty of Health Sciences, Hatay Mustafa Kemal University, between September-October 2026 with an enrollment of 133 healthy adult participants. The BARSE is a unidimensional scale consisting of 13 items. Participants are asked to rate their confidence in continuing to exercise under various challenging situations on a scale from 0% (not at all confident) to 100% (highly confident) in 10% increments. To establish construct validity and examine related health behaviors, participants will also complete several standardized tools: the Self-Rated Abilities for Health Practices Scale (SRAHP), the Exercise Benefits/Barriers Scale (EBBS), the Self-Perceived Barriers for Physical Activity Questionnaire (SPBPA), the Short Form Health Survey (SF-36), and the International Physical Activity Questionnaire-Short Form (IPAQ-SF).

Statistical Analysis The language adaptation will conduct using the standard translation and back-translation method. Content validity will be evaluated using the Davis technique. Construct validity will be assessed through factor analysis and correlation coefficients. For reliability analyses, the scales will be administered twice with a 15-day interval. Reliability will be determined by calculating Cronbach's alpha coefficient, corrected item-total correlations, and the Intraclass Correlation Coefficient (ICC). Potential differences between test and retest measurements will be evaluated using appropriate statistical tests.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Forward Translation and Synthesis: The original form will be translated into Turkish by two independent experts who are fluent in both languages and native speakers of Turkish. Following this, the research team will synthesize these translations into a single draft form. Backward Translation: The synthesized Turkish draft will be translated back into English by two independent translators who have never seen the original text before and are fluent in English. Expert Opinions: The Turkish version, the back-translated English version, and the original English version will be reviewed by 10 experts in the field of health sciences. Psychometric Analyses: The Turkish validity and reliability of the scale will be tested twice with a 15-day interval on 130 participants.

Tipo di studio

Osservativo

Iscrizione (Effettivo)

133

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Antakya
      • Hatay, Antakya, Turchia (Türkiye), 31000
        • Hatay Mustafa Kemal University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Department

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 18 anni a 45 anni (Adulto)

Accetta volontari sani

Sì

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione di probabilità

Popolazione di studio

The study will be conducted at the Faculty of Health Sciences, Hatay Mustafa Kemal University. It is planned to include 10 times the total number of items in the scale, and the Turkish validity and reliability of the scale, which has a total of 13 questions, will be tested on 130 participants. Simple random sampling will be applied to minimize selection bias.

Descrizione

Inclusion Criteria:

  • Healthy adults aged between 18 and 45 years.
  • Ability to read and write in Turkish.

Exclusion Criteria:

  • Having difficulties in reading and comprehending Turkish.
  • Presence of severe cognitive impairment.
  • Having a specific medical condition or physical disability that makes physical activity impossible.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Modelli osservazionali: OTHER
  • Prospettive temporali: PROSPECTIVE

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Healthy Adults

Healthy adults aged 18-45 who participated in the validity and reliability study of the Turkish version of BARSE.

Administration of the Turkish version of the Barrier-Specific Self-Efficacy Scale (BARSE) and other related questionnaires to investigate its validity and reliability.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Barrier Specific Self-Efficacy Scale (BARSE)
Lasso di tempo: To minimize recall bias, it will be administered twice, 15 days apart.

This is a psychometric tool that assesses an individual's belief in their ability to continue an exercise program in the face of various hindering situations that make exercise difficult, such as fatigue, bad weather, lack of time, or pain. It consists of 13 items and asks participants to rate their confidence in continuing exercise for each situation on a scale of 0 (I have no confidence at all) to 100 (I have great confidence).

To minimize recall bias, it will be administered twice, 15 days apart.
Self Rated Abilities for Health Practices Scale (SRAHP)
Lasso di tempo: To minimize recall bias, it will be administered twice, 15 days apart.

This scale was developed to assess individuals' self-efficacy perceptions regarding engaging in health-promoting behaviors. It consists of 28 items and covers four sub-dimensions: exercise, nutrition, health responsibility, and psychological well-being. The scale uses a 5-point Likert type, with items scored from "0 (never)" to "4 (completely)," resulting in a total score between 0 and 112; each sub-dimension score ranges from 0 to 28. Higher scores on the scale indicate increased self-efficacy in performing health-related practices.

To minimize recall bias, it will be administered twice, 15 days apart.
Exercise Benefits/Barriers Scale (EBBS)
Lasso di tempo: To minimize recall bias, it will be administered twice, 15 days apart.

This scale was developed to assess the perceived benefits and barriers to participation in exercise. The 43-item scale uses a 4-point Likert scale (Strongly agree to Strongly disagree). Exercise benefits are evaluated across five sub-dimensions: enriching life, psychological perspective, physical performance, social interaction, and preventative health; while exercise barriers are evaluated across three sub-dimensions: exercise environment, time expenditure, and physical strain. Sub-dimension scores are calculated by averaging the relevant items. The benefits subscale ranges from 29 to 116 points, and the barriers subscale ranges from 14 to 54 points. Higher benefit scores indicate greater perceived benefits, while higher barrier scores indicate fewer perceived barriers. The total EBBS score is calculated by summing the benefit and barrier scores.

To minimize recall bias, it will be administered twice, 15 days apart.
Self-Perceived Barriers for Physical Activity Questionnaire (SPBPA)
Lasso di tempo: To minimize recall bias, it will be administered twice, 15 days apart.

This is a 17-item self-report scale developed to assess perceived barriers to participation in physical activity. The scale consists of four sub-dimensions: body image and psychosocial anxiety, fatigue, responsibilities and lack of time, and environment and facilities. Items are scored on a Likert-type scale ranging from 0 (low) to 10 (high); each sub-dimension score is obtained by dividing the total score of the relevant item by the number of items. A higher score on the scale indicates a higher level of perceived barriers to participation in physical activity.

To minimize recall bias, it will be administered twice, 15 days apart.
The Short Form Health Survey (SF-36)
Lasso di tempo: To minimize recall bias, it will be administered twice, 15 days apart.

This is a 36-item self-assessment test designed to gather information about a person's health status. The questionnaire includes eight multi-item subscales assessing physical function, social functioning, role limitations due to physical problems, role limitations due to emotional problems, mental health, vitality, pain, and general health perception. The total score ranges from 0 to 100.

To minimize recall bias, it will be administered twice, 15 days apart.
The International Physical Activity Questionnaire- Short Form (IPAQ-SF)
Lasso di tempo: To minimize recall bias, it will be administered twice, 15 days apart.

The questionnaire, developed to determine physical activity levels, consists of 7 questions. It inquires about the time spent by individuals in vigorous, moderate, walking, and sitting activities for at least 10 minutes over the past 7 days. In the IPAQ, 8.0 METs are considered to be expended during vigorous physical activity, 4.0 METs during moderate physical activity, and 3.3 METs during walking. To score and determine the level of activity, the walking, moderate, and vigorous activity scores are added together to obtain a total physical activity score (MET-min/week). Scores are obtained by multiplying the standard values of the activities by the number of days per week and the number of hours per day these activities are performed. In the IPAQ, physical activity levels are classified as follows: Inactive (I) with a total physical activity score of 600 METs and below, Minimally Active (II) with a score between 600 and 3000 METs, and Active (III) with a total score above 3000 METs.

To minimize recall bias, it will be administered twice, 15 days apart.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 ottobre 2026

Completamento primario (Effettivo)

16 ottobre 2026

Completamento dello studio (Effettivo)

26 ottobre 2026

Date di iscrizione allo studio

Primo inviato

24 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

24 settembre 2026

Primo Inserito (Effettivo)

30 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

27 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

26 ottobre 2026

Ultimo verificato

1 ottobre 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • BARSE2026-01

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .