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The Validity and Reliability of the Turkish Version of the BBAQ

I

Istanbul Medeniyet University

Status

Enrolling

Conditions

Physical Inactivity
Health Knowledge, Attitudes, Practice

Study type

Observational

Funder types

Other

Identifiers

NCT06978686
2025/BBAQ

Details and patient eligibility

About

The Barriers to Being Active Quiz (BBAQ) was originally developed in English to identify barriers to physical activity. This study aims to translate and cross-culturally adapt the BBAQ into Turkish (BBAQ-T) and evaluate its psychometric properties.

Full description

The study involves the translation and cross-cultural adaptation of the BBAQ into Turkish and the assessment of its reliability and validity. A total of 210 healthy participants will be recruited. The adaptation process will follow a standardized back-translation method using two bilingual translators. A pilot study (n=15) will assess face validity, including linguistic clarity, conceptual relevance, and administration time. To evaluate test-retest reliability, participants will complete the BBAQ-T again within 5-7 days after the initial assessment. Internal consistency will be analyzed using Cronbach's alpha (α). Construct validity will be examined by correlating the BBAQ-T with the Turkish versions of the Self-Perceived Barriers for Physical Activity Questionnaire and the Short Form-12 (SF-12).

Enrollment

210 estimated patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged 18 years or older
  • Ability to read and write in Turkish
  • No visual or hearing impairments that would interfere with participation
  • Ability to follow simple instructions
  • Willingness to participate in the study

Exclusion criteria

  • Diagnosis of rheumatological conditions that may limit physical activity and are characterized by chronic inflammation and/or joint deformities (e.g., rheumatoid arthritis, ankylosing spondylitis, systemic lupus erythematosus, psoriatic arthritis)
  • Physical limitations due to neurological or orthopedic conditions (e.g., stroke, cerebral palsy, multiple sclerosis, limb amputation, or orthopedic surgery within the past six months)
  • History of psychiatric disorders that may impair cognitive functioning (e.g., schizophrenia, bipolar disorder, severe depression, attention deficit hyperactivity disorder)
  • Presence of any cognitive impairment

Trial design

210 participants in 1 patient group

Healthy volunteers
Description:
This group consists of healthy university students between the ages of 18 and 35 who voluntarily participate in the study.

Trial contacts and locations

2

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Central trial contact

EMEL METE, PhD

Data sourced from clinicaltrials.gov

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