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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05424341
Other study ID # Taliah Bashir Sindhu
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2022
Est. completion date December 1, 2022

Study information

Verified date April 2023
Source University of Lahore
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Previous studies has discussed the effects of muscle energy technique and counterstrain technique in upper trapezius and low back pain but no comparative study is found on planter fasciitis patients. In this study we are going to compare the effects of muscle energy technique and counterstrain technique with routine physical therapy in relation with pain, functional status and satisfaction level in planter fasciitis patients


Description:

Heel pain is one of the most prevalent musculoskeletal diseases of the lower limb, affecting both physically active and sedentary people. Amongst the possible causes, planter fasciitis is one of the most common cause of heel pain. Planter fasciitis is a degenerative syndrome resulting from the repeated injury at its origin on the calcaneus. Its most common symptom is discomfort in the plantar area of the foot and, more specifically, in the inferior part of the heel. It is frequently more intense while taking your first steps in the morning or after a period of physical inactivity, and it worsens with prolonged standing or weight-lifting activities. It is not frequently linked to nocturnal discomfort or paresthesia. Different physiotherapy treatment conventions help in pain relieving for example, rest, taping, stretching, orthosis-night brace, Silicon heel cups and myofascial release. This study will compare the effects of Muscle Energy Technique versus Counterstrain Technique in patients with plantar Fasciitis.


Recruitment information / eligibility

Status Completed
Enrollment 66
Est. completion date December 1, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years to 68 Years
Eligibility Inclusion Criteria: - Age 20 to 68 years. - Both male and female. - Patients are clinical diagnosed by the orthopedic surgeon. - Patients present with pain that persist for more than 4 weeks in heel and planter surface of foot. - Pain with the first steps after inactivity Exclusion Criteria: - • Patients with history of ankle and foot fracture. - Congenital or acquired deformity of ankle and foot. - Patients with arthritis. - Pervious history of surgery for planter fasciitis. - Patients use an assistive device for walking. - Patients use corticosteroid injection in heel.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Muscle Energy Technique
For Gastrocnemius muscle, subject will be in supine position keeping knee fully extended and therapist on affected side in walking position. The subject's ankle joint will be dorsiflexed until a resistance feel and will ask to hold this position and exert 20% of force towards plantar flexion for a period of 5 to 7 seconds. Resistance will be released and relaxation of 5 seconds will be given during which the ankle will was passively dorsiflexed to a new barrier. 5 repetitions will be given.
Counterstrain Technique
Therapist places thumb on tender point at plantar fascia insertion while patient in supine position with ipsilateral knee flexed. Plantar flex the toes and ankle while monitoring sore site with thumb, curling around tender point until monitoring thumb feels symptomatic relief. Supination/pronation of foot will be added if necessary. The position of ease will be maintained for 90 secs until tissues beneath monitoring thumb softens. Tender spot is re-evaluated once the foot is returned to neutral without moving the thumb. It will be repeated 3 times for 30 secs resting interval in-between

Locations

Country Name City State
Pakistan The University of Lahore Lahore Punjab

Sponsors (1)

Lead Sponsor Collaborator
University of Lahore

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Intensity Pain intensity will be measured by Visual Analogue Scale (VAS) Change in pain intensity will be measured at baseline, at end of first week, at end of second week
Primary Function Functional status will be measured by Foot and Ankle Ability Measure (FAAM) Change in Functional Status will be measured at baseline, at end of first week, at end of second week
Primary Satisfaction Level Satisfaction level will be measured by Short-Form Patient Satisfaction Questionnaire (PSQ-18) Level of satisfaction will be observed at end of First Session, at end of first week, at end of second week
See also
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