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Plantar FascitisNCT07078513

Active Release Technique Versus Strain-Counter Strain in Improving Pain and Function in Plantar Fasciitis

A study testing Active release Technique and Strain counter strain tecnhnique in people with Plantar Fascitis, run by Riphah International University at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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. Read more about this study

Who is it for?
Ages 25 to 45 years
Conditions the study is for
Plantar Fascitis
What is being tested?
Active release Technique and Strain counter strain tecnhnique
Could I receive a placebo?
No, everyone receives an active treatment
How many people
20 participants
Where
1 sitePakistan
Study dates
15 Aug 2025to 16 Jan 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 45 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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.

Who cannot join

  • Recent lower limb surgery.
  • Neurological disorders affecting gait or mobility.
  • Acute inflammatory conditions of the foot.

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Riphah international University Malakand Campus

    Chakdara, KPK, 18800

Other trials in Pakistan

About this study

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.

Read the detailed description

This randomized controlled trial investigates the comparative effectiveness of Active Release Technique (ART) and Strain-Counterstrain (SCS) in managing plantar fasciitis, a common cause of heel pain and functional limitation. Forty participants will be randomly assigned to two intervention groups, each receiving either ART or SCS over a four-week period, with sessions conducted three times per week. ART involves targeted pressure with active tissue movement to release adhesions, while SCS uses passive positioning to relieve muscle tension. The study will be conducted at Bacha Khan Medical Complex, Swabi. Data will be analyzed using appropriate statistical methods to determine the superior technique. The findings aim to support evidence-based manual therapy approaches in clinical physiotherapy practice.

Being tested
Active release Technique, Strain counter strain tecnhnique
Keywords
Plantar fasciitis, Chronic Plantar Fasciitis
Medical subject headings
Fasciitis, Plantar

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Active release TechniqueOther

    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 counter strain tecnhniqueOther

    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.

Study groups in NCT07078513
Study groupRoleWhat they receive
Active release TechniqueExperimentalParticipants 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.
Receives: Other: Active release Technique
Strain counter strain tecnhniqueExperimentalParticipants 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.
Receives: Other: Strain counter strain tecnhnique

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: four weeks

  2. 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.

    Measured: Four weeks

  3. 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.

    Measured: Four weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Jul 2025
  2. Study start15 Aug 2025
  3. Primary completion30 Dec 2025
  4. Study completion16 Jan 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
20 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07078513
Sponsor's protocol ID
REC-01016 Asad Zaman
Status last verified
Feb 2026
First submitted
14 Jul 2025
Last updated
19 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Active release Technique and Strain counter strain tecnhnique in people with Plantar Fascitis, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

NPRS (time frame: four weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Feb 2026.

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