Body Awareness Therapy in High Stressed Young Adults: Effects on Function, Balance, Sleep and Mood
Investigating the Effects of Body Awareness Therapy on Functional Capacity, Balance, Sleep Quality and Psychological State in Young Adults With High Stress Levels: A Randomized Controlled Trial
1 other identifier
interventional
62
1 country
1
Brief Summary
Body Awareness Therapy (BAT) is a holistic approach to human movement that considers the physical, physiological, psychological, and existential aspects of human existence. This planned randomized controlled study will be conducted on young adults with high stress levels. One group will be subjected to BAT and the other group will be the control group. The BAT exercises will be performed in supine, sitting and standing positions. In the BAT group, the exercises will be performed as a group exercise, not individually. After the initial evaluations in both the BAT and control groups, a re-evaluation will be performed at the end of 8 weeks. Functional capacity will be assessed with the 6-minute walk test, static balance with the single-leg balance test (eyes open-eyes closed), dynamic balance with the Y-balance test, psychological status with the Depression-Anxiety-Stress Scale-21 (DASS-21), and sleep quality with the Pittsburgh Sleep Quality Scale. BAT will be performed 2 days per week for 8 weeks and will be continued progressively. This study will examine the effects of BaT on functional capacity, balance, sleep quality, and psychological state in young adults with high stress levels.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
1 active site
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
Study Start
First participant enrolled
May 30, 2025
CompletedFirst Submitted
Initial submission to the registry
June 23, 2025
CompletedFirst Posted
Study publicly available on registry
July 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
February 28, 2026
CompletedDecember 31, 2025
December 1, 2025
6 months
June 23, 2025
December 26, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
6-Minute Walk Test
They will be asked to walk as fast as they can down a 30-meter straight corridor for 6 minutes.
8 weeks
Single Leg Stance Test
The maximum time that individuals can stand on one leg with eyes open and closed will be recorded.
8 weeks
Y Balance Test
During the test, 3 trials will be performed for each leg and the best score will be recorded (right anterior, left anterior, right posteromedial, left posteromedial, right posterolateral, left posterolateral). The maximum reach distance was recorded for each consecutive trial.
8 weeks
Depression Anxiety Stress Scale - 21
Psychological status will be evaluated. The total score for each heading ranges from 0 to 21. Higher total scores indicate higher depression, higher anxiety, and higher stress levels.
8 weeks
Pittsburgh Sleep Quality Index
Sleep quality will be evaluated. The 19 items measure seven subcomponents. Each question is scored between "0" and "3". The total score (0-21) is obtained by adding the seven subscores. According to the total score, those with a score of 5 and below are interpreted as having good sleep quality, and those with a score above 5 are interpreted as having poor sleep quality.
8 weeks
Secondary Outcomes (1)
International Physical Activity Questionnaire - Short Form
8 weeks
Study Arms (2)
Control Group
NO INTERVENTIONNo intervention
Intervention Group
EXPERIMENTALBody Awareness Therapy
Interventions
Eligibility Criteria
You may qualify if:
- Be between 20 and 30 years old
- Be literate
- Score 10 or above on the stress subscale of the Depression Anxiety Stress Scale -21
- Be willing to participate in the study voluntarily
You may not qualify if:
- Individuals with orthopedic, neurological, rheumatological, psychiatric, mental, or any systemic chronic diseases
- Those with cardiac problems that may prevent exercise
- Those suspected of being pregnant
- Individuals with malignancy
- Individuals with active infection
- Those who do not regularly attend the treatment program
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hatay Mustafa Kemal University, Faculty of Health Sciences, Physiotherapy and Rehabilitation Department
Hatay, Antakya, 31000, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Researcher, Head of Physiotherapy and Rehabilitation Department, Hatay Mustafa Kemal University
Study Record Dates
First Submitted
June 23, 2025
First Posted
July 1, 2025
Study Start
May 30, 2025
Primary Completion
November 30, 2025
Study Completion
February 28, 2026
Last Updated
December 31, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share
At the end of the study, with the acceptance of the article, the data requested by the reader can be shared with the approval of the authors.