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Clinical Trials in Turkey / NCT07688785
Recruiting Not applicable

Effects of Basic Body Awareness Therapy on Gait and Plantar Pressure in Healthy Young Adults

NCT07688785 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-29
Last updated
2026-07-15

Condition(s) studied

GaitBody Awareness

Investigational drug(s) / intervention(s)

Basic Body Awareness Therapy

Basic Body Awareness Therapy: The Basic Body Awareness Therapy program includes low-intensity physiotherapy exercises focused on awareness of contact with the floor, postural alignment, breathing-movement integration, weight transfer, trunk control, balance, and fluent movement quality.

Study summary

This interventional study will evaluate the effects of Basic Body Awareness Therapy (BBAT) on gait and plantar pressure outcomes in healthy young adults. Participants aged 18 to 25 years will receive a 12-week BBAT program delivered twice weekly by a physiotherapist trained in BBAT. Outcomes will be assessed at baseline, after the 12-week intervention, and at 3-month follow-up. The primary aim is to determine changes in gait speed and other spatiotemporal gait parameters during the 10-meter walk test. Secondary aims are to examine changes in static and dynamic plantar load distribution, right-left load sharing, and regional plantar pressure parameters. The study hypothesizes that BBAT will improve gait speed, reduce right-left differences in spatiotemporal gait parameters, improve bilateral load distribution during static stance and walking, and maintain these gains at 3-month follow-up.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Aged 18 to 25 years * Able to walk independently * No history of lower-extremity, spine, or balance-affecting trauma and/or surgery within the last 6 months * Not receiving regular Basic Body Awareness Therapy * Provides written informed consent Exclusion Criteria: * History of neurological, vestibular, or rheumatological disease * Acute musculoskeletal injury * Serious visual or hearing impairment * Pain, deformity, or assistive device use that may affect walking performance * Participation in a physiotherapy program and/or regular exercise program within the last 6 months * Any condition preventing regular participation in assessment or therapy sessions

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Health Sciences Ankara Turkey (Türkiye) Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07688785 on ClinicalTrials.gov ↗ ← All trials in Turkey