Instrument-Assisted Soft Tissue Mobilization on Gastrocnemius and Achilles Tendon in Plantar Fasciitis

Sponsor
Riphah International University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05775302
Collaborator
(none)
32
2
2
6
16
2.6

Study Details

Study Description

Brief Summary

Aim of this study is to compare the effects of instrument assisted soft tissue mobilization on gastrocnemius and Achilles tendon on pain,range of motion and foot disability.A randomized control trial that will include total 32 participants and divided into two groups.Patients in Group A will receive instrument assisted soft tissue mobilization of gastrocnemius and Group B will receive instrument assisted soft tissue mobilization of Achilles tendon. While conventional therapy will be given to both groups.Data collected will be analyzed through SPSS 25.

Condition or Disease Intervention/Treatment Phase
  • Other: IASTM of Gastrocnemius + Conventional therapy
  • Other: IASTM of AchillesTendon + Conventional Therapy
N/A

Detailed Description

Plantar fasciitis is typical condition that produces pain in the medial longitudinal arch of the foot.Repetitive traction stresses on the plantar fascia at its origin over the distal calcaneus obesity, the makeup of the feet, and lifestyle choices are all factors that might contribute to the development of PF.

Physiotherapy interventions includes stretching the gastrocnemius and soleus,dry needling, IASTM (instrument assisted soft tissue mobilisation), exercise therapy, ultrasound therapy, iontophoresis, laser therapy, splints, and taping.Use of Instrument-Assisted Soft Tissue Massage has increased in popularity, and the plantar fascia is a superficial tissue that may benefit from this treatment.The Graston Technique Instrument-assisted Soft Tissue Mobilisation not only increases blood flow and tissue healing to the area as well as breaking up soft tissue restrictions along with increase fibroblasts, mast cell production and phagocytes.

Previous literature were limited in sample size, and only immediate effects of these techniques were studied But this study opted for the long term use of graston technique on gastrocnemius in comparison on Achilles tendon. So the purpose of this study is to compare the effects of Graston technique instrument assisted soft tissue mobilization at gastrocnemius and Achilles tendon in patients with planter fascitis. It will add to the growing body of knowledge that if same technique on different soft tissues will yield comparable outcomes,which should be the alternate choice of therapy

Study Design

Study Type:
Interventional
Anticipated Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effects of Instrument-Assisted Soft Tissue Mobilization on Gastrocnemius and Achilles Tendon in Plantar Fasciitis
Anticipated Study Start Date :
Mar 15, 2023
Anticipated Primary Completion Date :
Aug 15, 2023
Anticipated Study Completion Date :
Sep 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: IASTM Gastrocnemius

Instrument assisted soft tissue mobilization on gastrocnemius Conventional therapy: Cryotherapy for 10 min stretching of calf and plantar fascia strengthning of intrinsic foot muscle

Other: IASTM of Gastrocnemius + Conventional therapy
The SWEEP technique will be performed downwards from the popliteal region to the Achilles tendon for 60 seconds, 30 times 12 sessions over a time frame of 4 weeks at a frequency of 3 sessions per week.

Active Comparator: IASTM Achillies Tendon

Instrument assisted soft tissue mobilization Achillies Tendon Conventional therapy: Cryotherapy for 10 min stretching of calf and plantar fascia strengthning of intrinsic foot muscle

Other: IASTM of AchillesTendon + Conventional Therapy
Participants will receive a maximum of 60 seconds<30 times 12 sessions over a time frame of 4 weeks at a frequency of 3 sessions per week.

Outcome Measures

Primary Outcome Measures

  1. Visual Analogue Scale [4 weeks]

    Visual analogue scale id used to measures pain intensity. It consists of a 10cm line, with two end points representing 0 ('no pain') and 10 (pain as bad as it could possibly be)

Secondary Outcome Measures

  1. Goniometer [4 weeks]

    Goniometer is used to measure the ROM of joints

  2. Foot and ankle disability index [4 weeks]

    Foot and Ankle Disability Index is a 34-item questionnaire divided into two subscales.

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Both male and female

  • Participants between age of 25 and 50 years

  • Patients with maximal pain located at the antero-medial aspect of the plantar surface of the calcaneus

  • Pain aggravated by passive dorsiflexion or standing/ walking on the big toe

  • Patients with pain on taking first step in the morning(18)

  • Patient volunteer to participate in the study and signed informed consent.

Exclusion Criteria:
  • Patient with history of musculoskeletal disorders.

  • Patient with any previous history of ankle or foot surgery.

  • Patient with history of ankle or foot fracture.

  • Patient with severe bone disorder (osteoporosis)

  • Patient with history of Venous insufficiency.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Adam Life Care Rawalpindi Punjab Pakistan 43600
2 Attock Hospital Rawalpindi Punjab Pakistan 43600

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Madiha Ali, MSOMPT, Riphah International University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT05775302
Other Study ID Numbers:
  • Parwasha Shoukat
First Posted:
Mar 20, 2023
Last Update Posted:
Mar 20, 2023
Last Verified:
Mar 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 Mar 20, 2023