NCT07045792

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

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
62

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

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

Completed
24 days until next milestone

First Submitted

Initial submission to the registry

June 23, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

July 1, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2026

Completed
Last Updated

December 31, 2025

Status Verified

December 1, 2025

Enrollment Period

6 months

First QC Date

June 23, 2025

Last Update Submit

December 26, 2025

Conditions

Keywords

Body Awareness TherapyStress LevelsPsychological StressBalanceSleep QualityFunctional CapacityPhysical TherapyPostural Balance

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 INTERVENTION

No intervention

Intervention Group

EXPERIMENTAL

Body Awareness Therapy

Procedure: Body Awareness Therapy

Interventions

Individuals trained for body awareness therapy.

Intervention Group

Eligibility Criteria

Age20 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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)

Location

MeSH Terms

Conditions

Stress, PsychologicalSleep Initiation and Maintenance Disorders

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesMental Disorders

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.

Locations