Effects of Active and PRT on Pain, Function and Temporospatial Gait Parameters in Runners With Plantar Fascitis

Sponsor
Riphah International University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06131762
Collaborator
(none)
26
1
2
12
2.2

Study Details

Study Description

Brief Summary

The study is randomized and single -blinded. Ethical approval is taken from ethical committee of Riphah International university Lahore.Participants who will meet criteria will be requested to give verbal consent and to sign written consent form. After signing consent form participants will be allocated to the group A and Group B by using computerized generated randomization. Group A will receive ultrasound then Active release technique while group B will receive ultrasound and Positional release technique for 4 weeks. Treatment sessions will be 12 sessions, 3 sessions per week on alternative days for 4 weeks

Condition or Disease Intervention/Treatment Phase
  • Other: Active release technique
  • Other: Positional release technique
N/A

Detailed Description

A single blinded randomized clinical trial will be conducted on 26 subjects diagnosed for planter fasciitis from Jawad Club Faisalabad and Alfatah Sports Club, Faisalabad by looking for symptoms and tenderness at heel as mentioned in inclusion criteria and will confirmed by windlass test. Participants who will meet criteria will be requested to give verbal consent and to sign written consent form. After signing consent form participants will be allocated to the group A and Group B by using computerized generated randomization. Group A will receive ultrasound then Active release technique while group B will receive ultrasound and Positional release technique for 4 weeks. Treatment sessions will be 12 sessions, 3 sessions per week on alternative days for 4 weeks. Pain will be measured by Numerical Pain Rating Scale (NPRS), Foot and ankle disability will be assessed by Foot Function Index (FFI), while gait parameters i.e. walking speed will be measured by 4-meter walking test, and step and stride length will be evaluated by measuring tape by taking foot prints before and after the 4 weeks of treatment period. Data will be analyzed through statistical package for the social sciences (SPSS) version 22.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
26 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized control trailRandomized control trail
Masking:
Single (Outcomes Assessor)
Masking Description:
the assessor who will take the reading is blind
Primary Purpose:
Other
Official Title:
Comparative Effects of Active and Positional Release Technique on Pain, Function and Temporospatial Gait Parameters in Runners With Plantar Fasciitis
Actual Study Start Date :
Feb 20, 2023
Anticipated Primary Completion Date :
Feb 20, 2024
Anticipated Study Completion Date :
Feb 20, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Active release technique

ART performed from long sitting position, the therapist started by shortening the muscle or fascia of affected limb then apply very specific pressure with hand as we stretch tissue is lengthened. Active movement is done whenever possible according to the instructions given by therapist. ART for 8-10 minutes will be given.

Other: Active release technique
This include active release technique for 4 weeks

Experimental: Positional release technique

Positional release technique where participant lie supine with the affected limb out of the plinth and then by application of brief mechanical pressure on tender point with one fingertip in order to determine tenderness. The foot should then be positioned, most probably into pure plantarflexion and gentle fine-tuned by rotation, until the score in the tender point has reduce by at least 70%. This position is held for 90 seconds with 3 repetitions i.e. total of 270 seconds was given.

Other: Positional release technique
This include positional release technique for 4 weeks

Outcome Measures

Primary Outcome Measures

  1. Foot Function [pre and 4 weeks post intervention]

    Foot function will be assessed by foot functional index scale Function will be assessed by Foot Function Index (FFI),

  2. Gait parameters [pre and 4 weeks post intervention]

    gait parameters i.e. walking speed will be measured by 4-meter walking test

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 30 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Male runners age between 18-30 years

  • Duration of running at least 6 months

  • Positive windlass test

  • Patients with unilateral or bilateral plantar fasciitis

Exclusion Criteria:
  • Recent accidental foot or ankle injury

  • Previous lower-body surgical intervention within 6 months

  • Recent fractures in the lower limb (femur, tibia, fibula or foot bones) within 6 months

  • Diagnosed musculoskeletal disorders (rheumatoid arthritis, calcaneal spurs)

  • Diagnosed neuropathy, local and systemic neurologic disorders (including sciatica, tarsal tunnel syndrome, nerve entrapment of abductor digiti minimi and posterior tibial

Contacts and Locations

Locations

Site City State Country Postal Code
1 Jawad club, Alfatah sports complex Faisalābad Punjab Pakistan 38000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Athar Azeem, Dpt, Investigator

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT06131762
Other Study ID Numbers:
  • REC/RCR & AHS/23/0432
First Posted:
Nov 14, 2023
Last Update Posted:
Nov 14, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Riphah International University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 14, 2023