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Not yet recruitingNCT07908602Updated Nov 2, 2026

Hip Muscle Strengthening and Calf Myofascial Release in Females With Chronic Plantar Fasciitis

An interventional study of Hip muscles Strengthening Exercises and Hip muscles Strengthening Exercises Combined with Calf Myofascial Release in Chronic Planter Fascitis, sponsored by University of Management and Technology Lahore. Not yet recruiting at 1 site in Pakistan. Open to female participants aged 25 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-11-02.

Sponsored by University of Management and Technology Lahore · Not applicable, Interventional, and Treatment

Updated Nov 2, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Randomized
Ages
25 Years to 45 Years
Sex
Female
01

Study summary

This study aims to compare the effects of hip muscle strengthening with and without myofascial release of the calf muscle on pain and disability in females with chronic plantar fasciitis.

Chronic plantar fasciitis is a common cause of heel pain and may lead to limitations in walking, daily activities, and functional performance. Factors such as calf muscle tightness, restricted ankle dorsiflexion, altered lower-limb biomechanics, and proximal hip muscle weakness may contribute to persistent symptoms. Although strengthening exercises and myofascial release have shown beneficial effects, limited evidence is available regarding the combined effect of hip strengthening and calf myofascial release in females with chronic plantar fasciitis.

The study will be conducted as a randomized clinical trial with a total sample of 34 females, aged 25-45 years, who meet the specified criteria for chronic plantar fasciitis. Participants will be randomly allocated into two groups. Group A will receive hip muscle strengthening exercises, while Group B will receive the same strengthening program combined with myofascial release of the calf muscles. Both groups will receive treatment three times per week for six weeks, for a total of 18 sessions.

The primary outcome measures will include the Numeric Pain Rating Scale (NPRS), Foot Function Index (FFI), and Morning First-Step Pain Visual Analogue Scale (VAS). Assessments will be performed at baseline and after completion of the six-week intervention.

02

Conditions studied

  • Chronic Planter Fascitis

Keywords

  • Hip muscle strengthening
  • myofascial release
  • chronic planter fasciitis
03

In context

Lead sponsor

University of Management and Technology Lahore is the lead sponsor of 34 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
25 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Participants fulfilling the diagnostic criteria for plantar fasciitis. Age between 25-45 years. NPRS score between >3-6. History of chronic plantar heel pain for at least 3 consecutive months. Positive Windlass Test. Morning first-step pain intensity >5 cm on a 10-cm Visual Analog Scale (VAS).

Exclusion criteria

Exclusion Criteria:

Recent history of foot, ankle, or lower limb surgery. Corticosteroid injection for plantar fasciitis within the previous three months.

Diagnosed neurological disorders affecting lower limb function. Pregnancy. Heel pain due to any other systemic inflammatory condition such as rheumatoid arthritis, gout, hyperuricemia (uric acid disorders), or other causes of heel pain.

Foot or ankle fracture within the previous six months. Participation in any structured physiotherapy program for plantar fasciitis during the previous month.

Presence of tarsal tunnel syndrome, Achilles tendon rupture, or other significant foot pathologies.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
34 participants (estimated)

Study arms

  • Experimental
    Arm 1: Hip muscles Strengthening Exercises

    Participants will receive hip abductor strengthening exercises three sessions per week for six weeks to improve pain and functional outcomes associated with chronic plantar fasciitis.

    Other: Hip muscles Strengthening Exercises

  • Active comparator
    Arm 2: Hip muscles Strengthening Exercises Combined with Calf Myofascial Release

    Participants will receive hip muscles strengthening exercises combined with myofascial release of the calf muscles three sessions per week for six weeks to evaluate the additional effects of calf myofascial release on pain and functional outcomes associated with chronic plantar fasciitis.

    Other: Hip muscles Strengthening Exercises Combined with Calf Myofascial Release

Interventions

  • OtherHip muscles Strengthening Exercises

    hip abductor strengthening exercises three sessions per week for six weeks

  • OtherHip muscles Strengthening Exercises Combined with Calf Myofascial Release

    hip muscles strengthening exercises combined with myofascial release of the calf muscles three sessions per week for six weeks

06

What researchers measure

Primary outcomes

  1. Numeric Pain Rating Scale (NPRS)

    The Numeric Pain Rating Scale (NPRS) will be used to assess the intensity of pain associated with chronic plantar fasciitis. It is an 11-point numerical scale ranging from 0 to 10, where 0 represents no pain and 10 represents the worst imaginable pain. Higher scores indicate greater pain intensity.

    Time frame: Baseline and after 6 weeks

  2. Foot Function Index (FFI)

    The Foot Function Index (FFI) will be used to assess foot-related pain, disability, and activity limitation in females with chronic plantar fasciitis. The questionnaire evaluates the impact of foot symptoms on functional activities. Higher scores indicate greater pain and functional limitations.

    Time frame: Baseline and after 6 weeks

  3. Morning First-Step Pain Visual Analog Scale (VAS)

    The Visual Analog Scale (VAS) will be used to assess pain experienced during the first steps taken in the morning after a period of rest. Participants will indicate their pain intensity on a 10-cm visual analog line, with one end representing no pain and the other representing the worst imaginable pain. Higher scores indicate greater morning first-step pain.

    Time frame: Baseline and after 6 weeks

07

Study locations

1 site
  • UMT
    Lahore, Punjab Province 54000, Pakistan
    • Fizza Masood Dr., MS-OMPT · Contactfizza.masood@umt.edu.pk · +923344318731
    • Rabia Jawa CoD Physical Therapy and Rehabilitation, MPhil PT · Contactrabia.jawa@umt.edu.pk · +923434570838
    • Sadia Riaz · Sub investigator
08

References and documents

Individual participant data

Plan to share: Yes — The results data collected , de-identified individual participant data will be shared.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form

Time frame: 6 months after the publication of the manuscript.

Access criteria: The data can be requested from the corresponding author.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2026; primary completion for Dec 2026, 2 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 26, 2026
First posted
Nov 2, 2026
StartEst.
Oct 27, 2026
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2026
Last update
Nov 2, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 2, 2026
Show all 1 update
  1. Nov 2, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07908602
Lead sponsor
University of Management and Technology Lahore
Responsible party
Fizza Masood (Assistant Professor, University of Management and Technology Lahore) — Principal investigator
First posted
Nov 2, 2026
Start date
Oct 27, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Nov 2, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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