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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05775302
Other study ID # Parwasha Shoukat
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 15, 2023
Est. completion date September 15, 2023

Study information

Verified date March 2024
Source Riphah International University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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


Recruitment information / eligibility

Status Completed
Enrollment 32
Est. completion date September 15, 2023
Est. primary completion date August 15, 2023
Accepts healthy volunteers No
Gender All
Age group 25 Years to 50 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

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.
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.

Locations

Country Name City State
Pakistan Adam Life Care Rawalpindi Punjab
Pakistan Attock Hospital Rawalpindi Punjab

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale 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) 4 weeks
Secondary Goniometer Goniometer is used to measure the ROM of joints 4 weeks
Secondary Foot and ankle disability index Foot and Ankle Disability Index is a 34-item questionnaire divided into two subscales. 4 weeks
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