Effects of Body Awareness Therapy on Physical and Psychosocial Outcomes in Adults With Asthma
Effect of Body Awareness Therapy on Physical and Psychosocial Outcomes in Adults With Asthma: A Randomized Controlled Trial
1 other identifier
interventional
67
0 countries
N/A
Brief Summary
This study aims to investigate the effects of Body Awareness Therapy on physical and psychosocial outcomes in adults with asthma. Asthma is a chronic respiratory condition that can affect breathing, physical activity, and emotional well-being. In addition to medical treatment, non-pharmacological approaches that support body awareness and breathing may help individuals manage their symptoms more effectively. Participants in this study will be randomly assigned to either a Body Awareness Therapy group or a control group receiving standard care. The Body Awareness Therapy program includes guided exercises focusing on posture, breathing, movement, and awareness of bodily sensations. The program will be delivered over several weeks by a trained physiotherapist. The main outcomes of the study include physical function, respiratory symptoms, quality of life, psychological well-being, and body awareness levels. The results of this study are expected to provide evidence on whether Body Awareness Therapy can be an effective supportive approach in asthma management and rehabilitation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable asthma
Started Feb 2026
Shorter than P25 for not_applicable asthma
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 31, 2026
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedFirst Posted
Study publicly available on registry
February 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedFebruary 13, 2026
February 1, 2026
2 months
January 31, 2026
February 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Six-Minute Walk Test Distance
Physical function will be assessed using the Six-Minute Walk Test (6MWT). Total walking distance covered in six minutes will be recorded. (Units of Measure: Meters)
Baseline (Week 0) and Post-intervention (Week 8)
Asthma Control Test Total Score
Asthma symptom severity will be assessed using the Turkish Asthma Control Test (T-ACT). The total questionnaire score will be analyzed.
Baseline (Week 0) and Post-intervention (Week 8)
Study Arms (2)
Body Awareness Therapy Group
EXPERIMENTALParticipants will receive a structured Body Awareness Therapy program delivered by a trained physiotherapist.
Standard Care Control Group
ACTIVE COMPARATORParticipants will receive standard medical care for asthma without additional body awareness intervention.
Interventions
A structured Body Awareness Therapy program delivered by a trained physiotherapist, including guided exercises focusing on breathing awareness, posture, gentle movement, and attention to bodily sensations.
Participants will continue their usual medical care for asthma without additional body awareness intervention.
Eligibility Criteria
You may qualify if:
- Adults aged between 18 and 65 years.
- Clinically diagnosed asthma confirmed by a physician.
- Stable asthma condition (no acute exacerbation in the last 4 weeks).
- Receiving regular medical treatment for asthma.
- Able to understand and follow instructions for the intervention.
- Willing to participate and provide written informed consent.
You may not qualify if:
- Diagnosis of chronic respiratory diseases other than asthma (e.g., COPD, bronchiectasis).
- Acute asthma exacerbation within the last 4 weeks.
- Severe cardiovascular, neurological, or musculoskeletal conditions that may limit participation in physical activity.
- Current participation in another structured exercise or rehabilitation program.
- History of major psychiatric disorders that may interfere with participation (e.g., psychotic disorders).
- Pregnancy.
- Cognitive impairment affecting the ability to follow instructions.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Recep Tayyip Erdogan Universitylead
- İstanbul Yeni Yüzyıl Üniversitesicollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
January 31, 2026
First Posted
February 13, 2026
Study Start
February 1, 2026
Primary Completion
April 1, 2026
Study Completion
May 1, 2026
Last Updated
February 13, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
Individual participant data (IPD) will not be shared publicly due to ethical and privacy considerations, as the data include sensitive personal and health-related information. Data will be used only for the purposes of the current study and stored in accordance with institutional and data protection regulations.