Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
NCT07229079

The Effectiveness of Basic Body Awareness Therapy in Individuals With Pes Planus

Led by Mardin Artuklu University · Updated on 2025-11-17

50

Participants Needed

1

Research Sites

47 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study investigates whether adding Basic Body Awareness Therapy (BBAT) to Short Foot Exercises (SFE) improves pes planus, balance, and body awareness in adults with flexible pes planus. Fifty participants aged 18-45 will be randomly assigned to either a BBAT + SFE group or an SFE-only control group. The interventions will last eight weeks with supervised sessions twice weekly and additional home exercises. Outcomes will be measured before, after, and two months post-intervention.

CONDITIONS

Official Title

The Effectiveness of Basic Body Awareness Therapy in Individuals With Pes Planus

Who Can Participate

Age: 18Years - 45Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-45 years
  • Willing to participate in the study
  • Diagnosed with flexible pes planus (Navicular Drop 210 mm and positive Jack's Toe Raise Test)
Not Eligible

You will not qualify if you...

  • Pain in lower extremity joints
  • Obesity (BMI >30)
  • Pregnancy
  • Systemic, neuromuscular, or neurological disorders
  • Posterior tibial tendon dysfunction (unable to perform heel-rise test)
  • History of lower limb surgery
  • Previous treatment for pes planus or use of foot orthoses
  • Lower extremity injury in past 6 months
  • Orthopedic conditions other than pes planus and mild hallux valgus (Manchester Scale C or D excluded)
  • Participation in regular exercise program in past 6 months
  • Prior personal experience with TBFT and/or short foot exercises

AI-Screening

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Trial Site Locations

Total: 1 location

1

Mardin Artuklu University

Mardin, Mardi̇n, Turkey (Türkiye)

Actively Recruiting

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Research Team

F

Fatma Betül Yardımcı

CONTACT

B

Bahar Anaforoglu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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