NCT06131762

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

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
26

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2023

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 20, 2023

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

November 9, 2023

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 14, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 20, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 20, 2024

Completed
Last Updated

December 29, 2023

Status Verified

December 1, 2023

Enrollment Period

1 year

First QC Date

November 9, 2023

Last Update Submit

December 26, 2023

Conditions

Keywords

painfunctions

Outcome Measures

Primary Outcomes (2)

  • Gait parameters

    gait parameters will be measured by 4-meter walking test

    pre and 4 weeks post intervention

  • Foot Function

    Foot function will be assessed by Foot Function Index (FFI),

    pre and 4 weeks post intervention

Study Arms (2)

Active release technique

EXPERIMENTAL

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

Positional release technique

EXPERIMENTAL

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

Interventions

This include active release technique for 4 weeks

Active release technique

This include positional release technique for 4 weeks

Positional release technique

Eligibility Criteria

Age18 Years - 30 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Male runners age between 18-30 years
  • Duration of running at least 6 months
  • Positive windlass test
  • Patients with unilateral or bilateral plantar fasciitis

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Jawad club, Alfatah sports complex

Faisalābad, Punjab Province, 38000, Pakistan

RECRUITING

Related Publications (5)

  • Brachman A, Sobota G, Marszalek W, Pawlowski M, Juras G, Bacik B. Plantar pressure distribution and spatiotemporal gait parameters after the radial shock wave therapy in patients with chronic plantar fasciitis. J Biomech. 2020 May 22;105:109773. doi: 10.1016/j.jbiomech.2020.109773. Epub 2020 Apr 3.

    PMID: 32279933BACKGROUND
  • Waclawski ER, Beach J, Milne A, Yacyshyn E, Dryden DM. Systematic review: plantar fasciitis and prolonged weight bearing. Occup Med (Lond). 2015 Mar;65(2):97-106. doi: 10.1093/occmed/kqu177. Epub 2015 Feb 17.

    PMID: 25694489BACKGROUND
  • Tong KB, Furia J. Economic burden of plantar fasciitis treatment in the United States. Am J Orthop (Belle Mead NJ). 2010 May;39(5):227-31.

    PMID: 20567740BACKGROUND
  • Thong-On S, Bovonsunthonchai S, Vachalathiti R, Intiravoranont W, Suwannarat S, Smith R. Effects of Strengthening and Stretching Exercises on the Temporospatial Gait Parameters in Patients With Plantar Fasciitis: A Randomized Controlled Trial. Ann Rehabil Med. 2019 Dec;43(6):662-676. doi: 10.5535/arm.2019.43.6.662. Epub 2019 Dec 31.

    PMID: 31918529BACKGROUND
  • Fabrikant JM, Park TS. Plantar fasciitis (fasciosis) treatment outcome study: plantar fascia thickness measured by ultrasound and correlated with patient self-reported improvement. Foot (Edinb). 2011 Jun;21(2):79-83. doi: 10.1016/j.foot.2011.01.015. Epub 2011 Mar 12.

    PMID: 21398108BACKGROUND

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Athar Azeem, Dpt

    Investigator

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Malia younas, Ms DPT

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
the assessor who will take the reading is blind
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Randomized control trail
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 9, 2023

First Posted

November 14, 2023

Study Start

February 20, 2023

Primary Completion

February 20, 2024

Study Completion

February 20, 2024

Last Updated

December 29, 2023

Record last verified: 2023-12

Data Sharing

IPD Sharing
Will not share

Locations