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Effects of Basic Body Awareness Therapy on Pain, Work Stress, Quality of Life, and Eating Attitudes in Adults

Study acronym: TBFT-WELL
StatusActive, Not Recruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 1 of 2 changed
See other at-risk trials from Hitit University

Record History

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  1. Primary endpoint(s) modified Show 4 more changesShow less
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: details revised at 1 of 3 entries
    • Study description shortened, about 14 words
    • Publications: details revised at 7 of 8 entries
  2. Secondary endpoints: details revised at 2 of 3 entries
    • Study title shortened, about 4 words
    v2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This study will examine the effects of a 10-week Basic Body Awareness Therapy (BBAT) program on pain, work-related stress, quality of life, and eating attitudes in healthy adults working at a university. Twenty participants aged 25-55 will be randomly assigned to either an intervention group, receiving one BBAT group session per week for 12 weeks, or a control group, receiving no intervention during the same period. Participants in both groups will be assessed before and after the 10-week period using validated scales: the Visual Analog Scale and McGill Pain Questionnaire for pain, the Job Content Questionnaire (work stress scale) for work-related stress, the Short Form-36 for quality of life, and the Eating Attitudes Test-26 for eating attitudes. In addition, participants in the intervention group will keep a session-by-session exercise diary, and their written reflections will be used to provide qualitative insight into how they experienced the intervention, complementing the quantitative results. This combination of quantitative and qualitative data collection is intended to provide both statistical evidence and a richer understanding of participants' experiences with the therapy.
Trial Details
NCT Number NCT07736599
Lead Sponsor Hitit University
Collaborators: Amasya University
Conditions
(from sponsor)		 Healthy Volunteers
Related terms Occupational Stress, Pain
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov