Examining the Effects of Basic Body Awareness Therapy on Quality of Life, Pain, Work Stress, and Eating Attitudes in Adult Individuals
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 20
- Locations
- 1
- Primary Endpoint
- Change in Pain Intensity (Visual Analog Scale)
Study Overview
Brief Summary
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.
Detailed Description
Modern working conditions - prolonged desk-based work, high mental workload, insufficient physical activity, and psychosocial stress - are thought to reduce body awareness and contribute to the development of chronic pain, elevated stress levels, and disordered eating attitudes. Basic Body Awareness Therapy (BBAT) is a movement-awareness-based physiotherapy approach, originating in Sweden in the late 1970s-1980s from the work of psychoanalyst and movement educator Jacques Dropsy, which aims to help individuals consciously perceive and reinterpret bodily sensations. BBAT incorporates core movement principles such as balance, free breathing, coordination, and awareness, delivered through simple, gentle, and safe movements performed in lying, sitting, standing, and walking positions, as well as paired exercises. The approach has been applied across a range of conditions, including chronic pain, psychosomatic disorders, and eating disorders, with prior studies suggesting potential benefits for emotion regulation, self-esteem, and quality of life, and for supporting a healthier relationship with the body in disordered eating populations.
While previous research has examined the relationship between body awareness therapy and pain, work stress, eating attitudes, and quality of life separately, few studies have examined these outcomes jointly within a single controlled trial. This study addresses that gap using a two-arm, parallel-group, randomized controlled design.
Participants will be academic staff at Amasya University, aged 25-55, who do not currently participate in a regular structured exercise program (e.g., yoga, pilates). Individuals with a diagnosed chronic illness or those on regular medication will be excluded. Participation is voluntary, and written informed consent will be obtained prior to enrollment. Baseline assessments will be conducted before randomization.
Participants will be randomly assigned in a 1:1 ratio to an intervention group or a no-intervention control group (10 participants per group; 20 total). The intervention group will receive one 60-minute BBAT group session per week for 12 weeks, conducted in a university exercise room at room temperature. Sessions will include supine awareness and breath-focused exercises, midline awareness exercises (bringing the legs together), symmetric, asymmetric, and star-shaped stretches, breath-coordinated opening/closing movements, seated balance exercises, standing weight-shift and rhythmic movement exercises, rotational coordination, wave-like movement, pushing exercises, various walking exercises, "cat walk" massage, and a closing meditation. The control group will not receive any intervention during the same 12-week period. Participants in either group who miss two consecutive weekly sessions, or who begin another treatment program during the study, will be withdrawn from the study.
Quantitative outcomes will be assessed at baseline and after the 12-week period in both groups using the following validated instruments: the Visual Analog Scale (VAS) and the Short-Form McGill Pain Questionnaire for pain intensity and quality; the Job Content Questionnaire (Job Stress Scale, Karasek et al., adapted into Turkish by Demiral et al., 2007) for work-related stress (workload, job control, and social support subscales); the Short Form-36 (SF-36) for health-related quality of life across eight subdomains; and the Eating Attitudes Test-26 (EAT-26) for disordered eating attitudes, with a cutoff score of 20 indicating attitudes consistent with disordered eating risk.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Single (Outcomes Assessor)
Masking Description
Due to the nature of the intervention (a group-based movement therapy), participants and the person delivering the BBAT sessions cannot be blinded to group assignment. However, the researcher(s) responsible for administering and scoring the outcome measures (VAS, McGill Pain Questionnaire, SF-36, Job Content Questionnaire, EAT-26) and analyzing the exercise diary/qualitative data will be blinded to group allocation where feasible, to reduce assessment bias.
Eligibility Criteria
- Ages
- 25 Years to 55 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Employed as academic staff at Amasya University
- •Not currently participating in a regular structured exercise program (e.g., yoga, pilates)
Exclusion Criteria
- •Diagnosed chronic illness
- •Regular use of medication
- •Missing two consecutive weekly sessions during the study (applies to -intervention group; results in withdrawal)
- •Beginning another treatment program during the study period
Arms & Interventions
Basic Body Awareness Therapy (BBAT)
Participants in this arm will receive one 60-minute Basic Body Awareness Therapy group session per week for 10 weeks, conducted in a university exercise room. Sessions include supine awareness and breath-focused exercises, midline awareness, symmetric/asymmetric/star-shaped stretches, breath-coordinated movement, seated balance exercises, standing weight-shift and rhythmic movement exercises, rotational coordination, wave-like movement, pushing exercises, walking exercises, "cat walk" massage, and closing meditation. Participants will complete a structured exercise diary after each session.
Intervention: Basic Body Awareness Therapy (BBAT) (Behavioral)
Control
Participants in this arm will not receive any intervention during the 12-week study period. They will undergo the same baseline and post-study (week 12) assessments as the intervention group, without participating in BBAT sessions or keeping an exercise diary.
Outcomes
Primary Outcomes
Change in Pain Intensity (Visual Analog Scale)
Time Frame: Baseline and Week 10
Pain intensity will be assessed using the Visual Analog Scale (VAS), a 0-10 self-reported scale, with higher scores indicating greater pain intensity.
Change in Pain Quality and Intensity (Short-Form McGill Pain Questionnaire)
Time Frame: Baseline and Week 10
Pain will be assessed using the Turkish-validated Short-Form McGill Pain Questionnaire (SF-MPQ), which yields a total score ranging from 0 to 45, combining sensory and affective pain descriptors, where higher scores indicate greater pain severity (worse outcome).
Secondary Outcomes
- Change in Health-Related Quality of Life (Short Form-36)(Baseline and Week 10)
- Change in Work-Related Stress (Job Content Questionnaire / Job Stress Scale)(Baseline and Week 10)
- Change in Eating Attitudes (Eating Attitudes Test-26)(Baseline and Week 10)
Investigators
Ertugrul Deniz Kose
Assist. Prof.
Hitit University
