Effects of Short Foot Exercise on Knee Pain, Muscle Tone, Balance, and Quality of Life in Flexible Flatfoot Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorSahmyook University

About this trial

This study was a clinical trial to investigate the effects of Short Foot Exercise (SFE) and standard physical therapy on knee muscle tone, knee pain and function, balance ability, and quality of life in adults with flexible flat feet and knee pain.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

BMI (Body Mass Index): If between 18 and 25 kg/m²

Litigation period: If knee pain lasted for more than 6 weeks

Navicular drop test: If it was 10 mm or more

Numerical assessment scale: If knee pain was 4 or more

Disqualifiers

History of knee surgery: If you have had knee surgery

Treatment history: If you have received physical therapy for knee pain in the 4 weeks before the start of the study

Mental status: If you have a psychological disorder that may interfere with your participation in the study

Injury status: If you have a current serious injury affecting the lower extremity joints and foot

Trial design

Design model

Parallel

Treatments tested in this trial

  • Short Foot Exercise

    Behavioral

    * Description: Short Foot Exercise is a therapeutic exercise designed to strengthen intrinsic foot muscles and improve medial longitudinal arch stability. * Procedure: Participants will perform Short Foot Exercise twice daily, five times per week for four weeks. The exercise consists of progressive phases, starting with basic foot activation and advancing to resistance-based strengthening using bands. * Purpose: To determine if strengthening the foot's intrinsic muscles positively impacts knee pain, muscle function, and balance in individuals with flexible flatfoot.

  • Conventional Physical Therapy

    Behavioral

    * Description: Standard non-invasive physical therapy aimed at reducing knee pain, improving muscle relaxation, and enhancing lower limb function. * Procedure: Participants will receive twice-weekly conventional physical therapy for ten minutes per session over four weeks. Treatment includes soft tissue mobilization, muscle relaxation techniques, and neuromuscular stimulation, as appropriate for knee pain relief. * Purpose: To evaluate its effectiveness as a standalone treatment compared to the addition of Short Foot Exercise.

Treatment groups

44 Participants
are divided into 2 treatment groups
Group A: Short Foot Exercise + Conventional Physical TherapyExperimental treatment 2 interventions
Group B: Conventional Physical TherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Change in Knee Muscle Tension from Baseline to 4 Weeks (Measured by Myoton Pro - Frequency in Hz)

* Description: This outcome measure assesses changes in muscle tension (tone) in the knee region before and after the intervention. * Measurement Tool: Myoton Pro * Unit of Measure: Frequency (Hz) * Assessment Method: Myoton Pro applies a gentle mechanical impulse to the skin overlying the Vastus Medialis, Biceps Femoris, Gastrocnemius Medialis, and Tibialis Anterior muscles, recording oscillation frequency as an indicator of muscle tone.

Time frame
From enrollment to the end of treatment at 4 weeks
2

Change in Knee Muscle Stiffness from Baseline to 4 Weeks (Measured by Myoton Pro - Stiffness in N/m)

* Description: This measure evaluates changes in muscle stiffness, reflecting muscle resistance to external force. * Measurement Tool: Myoton Pro * Unit of Measure: Newton per meter (N/m) * Assessment Method: Stiffness is quantified by Myoton Pro by applying a controlled impulse and measuring the muscle's resistance to deformation.

Time frame
From enrollment to the end of treatment at 4 weeks
3

Change in Knee Muscle Elasticity from Baseline to 4 Weeks (Measured by Myoton Pro - Logarithmic Decrement)

* Description: This measure evaluates changes in muscle elasticity, which indicates the muscle's ability to return to its original shape after deformation. * Measurement Tool: Myoton Pro * Unit of Measure: Logarithmic decrement * Assessment Method: The Myoton Pro records how quickly oscillations in the muscle dampen after a mechanical impulse, representing its elasticity.

Time frame
From enrollment to the end of treatment at 4 weeks

Secondary outcomes

1

Change in Dynamic Balance from Baseline to 4 Weeks (Measured by Y-Balance Test - Reach Distance in cm)

* Description: This measure assesses changes in lower limb balance and stability using the Y-Balance Test (YBT). * Measurement Tool: Y-Balance Test (YBT) * Unit of Measure: Reach distance (cm) * Assessment Method: Participants will perform three reach directions (anterior, posteromedial, posterolateral) while maintaining single-leg stance. The maximum reach distance for each direction is recorded and averaged.

Time frame
From enrollment to the end of treatment at 4 weeks
2

Change in Quality of Life from Baseline to 4 Weeks (Measured by EQ-5D-5L - Score on a 5-Dimension Scale)

* Description: This outcome measure evaluates self-reported quality of life in five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. * Measurement Tool: EQ-5D-5L * Unit of Measure: Score on a 5-Dimension Scale * Assessment Method: Participants rate their health status on a 5-level Likert scale (1 = No problems, 5 = Extreme problems). A total EQ-5D-5L index score is calculated using a weighted algorithm.

Time frame
From enrollment to the end of treatment at 4 weeks
3

Change in Knee Pain from Baseline to 4 Weeks (Measured by WOMAC Pain Subscale - Score on a 5-Point Likert Scale)

* Description: This measure evaluates knee pain severity before and after treatment. * Measurement Tool: Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) - Pain Subscale * Unit of Measure: Score on a 5-Point Likert Scale * Assessment Method: Participants rate pain intensity across five activities (e.g., walking, climbing stairs) using a 0-4 scale (0 = No pain, 4 = Extreme pain).

Time frame
From enrollment to the end of treatment at 4 weeks
4

Change in Knee Function from Baseline to 4 Weeks (Measured by WOMAC Function Subscale - Score on a 5-Point Likert Scale)

* Description: This measure assesses changes in functional ability and movement limitations. * Measurement Tool: WOMAC - Function Subscale * Unit of Measure: Score on a 5-Point Likert Scale * Assessment Method: Participants rate functional difficulty in 17 daily activities (e.g., rising from a chair, bending) on a 0-4 scale (0 = No difficulty, 4 = Extreme difficulty).

Time frame
From enrollment to the end of treatment at 4 weeks

Other outcomes

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