Effect of Selected Rehabilitation Program in Patients With Plantar Fasciitis

NCT ID: NCT06456944

Last Updated: 2025-07-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-06-15

Study Completion Date

2025-04-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will be done to investigate the effect of the selected rehabilitation program for PF on plantar fascia thickness, clinical outcomes such as pain, foot function, dorsiflexion ROM and pressure pain threshold and alignment such as rearfoot eversion angle and foot posture index in patients with PF.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Plantar fasciitis (PF), which constitutes approximately 15% of all foot disorders, is the most prevalent cause of heel pain. It is a long-term degenerative process that is impacted by subtalar pronation and pes planus. One million US patients saw primary care physicians with PF between 1995 and 2000. There is not enough data to determine the best physical therapy management techniques for individuals with heel pain, despite the existence of multiple successful treatment approaches. this study investigated at how a mechanically based rehabilitation program affected patients with PF in terms of foot alignment, plantar fascia thickness, pain, pressure pain threshold, ROM and foot function. The approach included strengthening the plantar intrinsic muscles of the foot, plantar fascia specific stretching and Achilles tendon stretching, and passively correcting the pathomechanics of the foot by low dye tapping and high load resistance exercise for Achilles tendon and windlass mechanism

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Plantar Fascitis Plantar Fasciitis, Chronic Heel Pain Syndrome

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants
double blinded randomized controlled trial (participants blinded to the intervention and statistician blinded to group assignment)

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

selected rehabilitation program

involves 24 patients and will be given the selected rehabilitation program involving (self-stretching exercise, mobilization of the ankle and subtalar, rigid tape and unilateral heel raising exercise 3 times per week for 8 weeks.

Group Type EXPERIMENTAL

stretching exercises

Intervention Type OTHER

stretching exercises of the plantar fascia, gastrocnemius and soleus

rigid tape

Intervention Type OTHER

low-dye tapping will be done to provide mechanical correction to plantar fascia and medial longitudinal arch

mobilization

Intervention Type OTHER

mobilization techniques for the talocrural joint in weight bearing and non-bearing positions and subtalar joint

strengthening exercise

Intervention Type OTHER

strengthening exercise of the plantar intrinsic muscles using short foot exercise and strengthening of the Achilles tendon and windlass mechanism using unilateral heel raise exercises

traditional program

involves 24 patients and will be given the traditional program involving (self-stretching exercise, mobilization of the ankle and subtalar, plantar fascial release and ultrasonic therapy 3 times per week for 8 weeks.

Group Type EXPERIMENTAL

stretching exercises

Intervention Type OTHER

stretching exercises of the plantar fascia, gastrocnemius and soleus

ultrasound

Intervention Type DEVICE

therapeutic ultrasound upon the most painful point on the medial calcaneal tubercle. The parameters involved a pulsed mode (duty cycle 50%) using an intensity of 1.5 W/cm2 and a 1 MHz of frequency for 5 minutes

mobilization

Intervention Type OTHER

mobilization techniques for the talocrural joint in weight bearing and non-bearing positions and subtalar joint

myofascial release

Intervention Type OTHER

deep tissue release of the plantar fascia and flexor hallucis longus in a stretched position of the plantar fascia

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

stretching exercises

stretching exercises of the plantar fascia, gastrocnemius and soleus

Intervention Type OTHER

ultrasound

therapeutic ultrasound upon the most painful point on the medial calcaneal tubercle. The parameters involved a pulsed mode (duty cycle 50%) using an intensity of 1.5 W/cm2 and a 1 MHz of frequency for 5 minutes

Intervention Type DEVICE

rigid tape

low-dye tapping will be done to provide mechanical correction to plantar fascia and medial longitudinal arch

Intervention Type OTHER

mobilization

mobilization techniques for the talocrural joint in weight bearing and non-bearing positions and subtalar joint

Intervention Type OTHER

myofascial release

deep tissue release of the plantar fascia and flexor hallucis longus in a stretched position of the plantar fascia

Intervention Type OTHER

strengthening exercise

strengthening exercise of the plantar intrinsic muscles using short foot exercise and strengthening of the Achilles tendon and windlass mechanism using unilateral heel raise exercises

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Plantar medial heel pain: most noticeable with initial steps after a period of inactivity, but also worse following prolonged weight-bearing
* Pain with palpation of the proximal insertion of the plantar fascia
* Positive windlass test
* flat foot posture utilizing the foot posture index
* age range from 40 to 60 years

Exclusion Criteria

* tarsal tunnel syndrome
* atrophy of the fat pad.
* diabetic patients or patients with rheumatoid arthritis
* corticosteroid injection over the last sex months
Minimum Eligible Age

40 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Horus University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mohamed Ramadan Ibraheem Ramadan

principle investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Mohamed Ramadan Ibraheem, Assistant lecturer

Role: PRINCIPAL_INVESTIGATOR

Horus University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Outpatient clinic, Faculty of Physical Therapy, Horus University, Egypt

Damietta, , Egypt

Site Status

out-patient clinic, Faculty of Physical Therapy, Horus university

Damietta, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Mohamed PHD

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.