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Efficacy of the Functional Mobilization Approach in Young Adults with Anterior Knee Pain: A Randomized Clinical Trial

Phase 2/3
Completed
Conditions
Bilateral primary osteoarthritis of knee, Patellofemoral pain syndrome due to foot hyperpronation,
Registration Number
CTRI/2018/02/011796
Lead Sponsor
Sharda University and Hospital
Brief Summary

Foot hyperpronation is an abnormal inward rotation of the subtalar joint. Its relation to patellofemoral pain syndrome and was the focus of this study.

This study employed a three dimensional functional manual therapy approach (A combination of Functional joint mobilization, Proprioceptive Neuromuscular Facilitation, and functional soft tissue mobilization) to  treat and adjust both soft and bony tissue involved and the use of full length medial wedge insoles.

**Aim and objectives**:

- To investigate the clinical efficacy of functional manual therapy approach of foot and ankle along with routine exercises with respect to pain and function in these subjects.

- To find out if there’s a significant difference in pain and function with regard to using functional manual therapy of foot and ankle as treatment for patellofemoral pain syndrome

- To improve knee pain and lower limb function in individuals with patellofemoral pain syndrome

- To compare the clinical efficacy of functional manual therapy with full flange medial raise insoles in these subjects

**Null Hypothesis:** Functional manual therapy of foot and ankle will not improve pain and function in young adults with patellofemoral pain syndrome.

**Alternate Hypothesis:** Functional manual therapy of foot and ankle will improve pain and function in young adults with patellofemoral pain syndrome.

At the end of the study, the null hypothesis was rejected.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
60
Inclusion Criteria
  • 1.Clinically diagnosed cases of patellofemoral pain syndrome 2.
  • Presence of unilateral or bilateral foot hyperpronation 3.
  • Duration of PFPS must be more than three weeks (chronic).
Exclusion Criteria
  • 1.Defined injury or pathological conditions of the knee and foot structures (bursitis, tendinopathies, ligament sprains or instability, menisci injuries, dislocations) 2.
  • History of ankle and/or foot surgery 3.Severe or advanced knee osteoarthritis diagnosed based on clinical and radiological assessment 4.
  • Autoimmune diseases such as rheumatoid arthritis or systemic lupus erythematosus 5.
  • Leg length discrepancy of more than 1 inch 6.
  • Previous physiotherapy treatment (such as exercise therapy, orthosis, mobilization) in the past 12 months 7.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Pain using the Numeric Pain Rating Scale (0 to 10. Lower scores represent better results)Scores taken on first day and on last day (after three months)
2. Foot posture using the Foot Posture Index. Positive values indicate hyperpronationScores taken on first day and on last day (after three months)
3. Functional status of the lower extremity using the Lower Extremity Functional Scale with scores from 0 to 80. Higher scores represent better results.Scores taken on first day and on last day (after three months)
Secondary Outcome Measures
NameTimeMethod
Functional Tests1. Squatting with ability to keep heels on floor

Trial Locations

Locations (1)

Sharda Hospital

🇮🇳

Nagar, UTTAR PRADESH, India

Sharda Hospital
🇮🇳Nagar, UTTAR PRADESH, India
Lili Kalumyana Silumesii
Principal investigator
8800928706
silumesiilili@gmail.com

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