Active Release Technique Versus Strain-Counter Strain in Improving Pain and Function in Plantar Fasciitis
1 other identifier
interventional
20
1 country
1
Brief Summary
This randomized controlled trial compares the effectiveness of Active Release Technique (ART) and Strain-Counterstrain (SCS) in treating plantar fasciitis. Forty participants will be divided into two groups receiving either ART or SCS over a four-week period. The study aims to identify the more effective manual therapy technique for reducing pain and improving function in patients with plantar fasciitis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Aug 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 14, 2025
CompletedFirst Posted
Study publicly available on registry
July 22, 2025
CompletedStudy Start
First participant enrolled
August 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 16, 2026
CompletedFebruary 19, 2026
February 1, 2026
5 months
July 14, 2025
February 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
NPRS
The Numeric Pain Rating Scale (NPRS) is a 0 to 10 self-reported scale used to assess pain intensity, where 0 = no pain and 10 = worst possible pain. It is a simple, reliable tool commonly used in clinical trials to measure pain levels before and after interventions.
four weeks
Foot Function Index (FFI)
Functional mobility will be assessed using the Foot Function Index (FFI), a validated self-reported questionnaire designed to measure the impact of foot pathology on pain, disability, and activity limitation in daily life.
Four weeks
Goniometer
a reliable and widely used clinical tool that measures joint angles in degrees. It helps quantify movement limitations and improvements in specific planes, such as flexion, extension, abduction, and rotation.
Four weeks
Study Arms (2)
Active release Technique
EXPERIMENTALParticipants in this group will receive Active Release Technique (ART), a manual therapy approach focused on relieving soft tissue restrictions. The therapist will apply targeted pressure to areas of adhesion while the patient actively moves the affected tissue through its full range of motion. Each session will include approximately 30 repetitions and will be conducted three times per week for four weeks. This technique aims to restore normal tissue mobility and reduce pain.
Strain counter strain tecnhnique
EXPERIMENTALParticipants in this group will receive Strain-Counterstrain (SCS), a gentle manual therapy technique designed to reduce muscle tension and pain. The therapist will passively position the patient into a position of maximal comfort, targeting specific tender points. This position is held for approximately 90 seconds while maintaining light pressure, allowing the muscle and fascia to relax. Sessions will be conducted three times per week for four weeks, aiming to restore tissue balance and reduce discomfort.
Interventions
Active Release Technique (ART) is a hands-on manual therapy that targets soft tissue restrictions by combining precise pressure with patient-assisted movement. It helps break down adhesions, improve mobility, and reduce pain by restoring normal tissue function.
Strain-Counterstrain is a gentle, passive manual therapy that relieves muscle tension by positioning the body in a pain-free, comfortable posture. The therapist holds this position for about 90 seconds while applying light pressure to tender points, allowing the muscle and fascia to relax and reset.
Eligibility Criteria
You may qualify if:
- Patients age 25-45 years diagnosed with plantar fasciitis.
- Chronic plantar fasciitis (symptoms lasting more than 3 months).
- Ability to participate in active movement for ART.
You may not qualify if:
- Recent lower limb surgery.
- Neurological disorders affecting gait or mobility.
- Acute inflammatory conditions of the foot.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Riphah international University Malakand Campus
Chakdara, KPK, 18800, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Zavata Afnan, MS NMPT
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 14, 2025
First Posted
July 22, 2025
Study Start
August 15, 2025
Primary Completion
December 30, 2025
Study Completion
January 16, 2026
Last Updated
February 19, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share