Graston vs Manual Myofascial Release Technique in Piriformis Syndrome.

Sponsor
Riphah International University (Other)
Overall Status
Completed
CT.gov ID
NCT04588779
Collaborator
(none)
30
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2
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3.6

Study Details

Study Description

Brief Summary

The objective of our study is to compare the effects of Graston and manual myofascial release technique on pain, muscle length and functional status in patients with Piriformis syndrome.

Condition or Disease Intervention/Treatment Phase
  • Other: Graston
  • Other: Manual myofascial release
N/A

Detailed Description

In 2019, a study was conducted to conclude the effectiveness of Passive stretching v/s Myofascial release in improving Piriformis flexibility in females. They reported that myofascial release was more valuable than passive stretching exercises in enhancing piriformis flexibility in patients with piriformis tightness.

According to another study in 2018, after a single treatment, compressive myofascial release showed more improvement in ankle dorsiflexion than Graston technique, in participants with decrease dorsiflexion range.

In 2016, a study reported the effects of the Graston technique and general exercise in patients with chronic low back pain. Graston group showed greater improvement in pain and range of motion in patients with chronic low back pain.

According to a study conducted in 2014, self-myofascial release was more effective than Graston technique in improving knee joint flexibility, hamstring, and quadriceps strength.

In 2011, a study evaluated the effectiveness of deep soft tissue mobilization techniques and stretching exercises in piriformis syndrome and found that the deep soft tissue mobilization techniques along with stretching exercises significantly improved the piriformis syndrome.

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Both groups were treated simultaneously with their specified treatment techniques within given duration.Both groups were treated simultaneously with their specified treatment techniques within given duration.
Masking:
Single (Participant)
Masking Description:
Participants did not know which treatment techniques are given in the specified groups.
Primary Purpose:
Treatment
Official Title:
Comparison of Graston and Manual Myofacial Release Technique in Patients With Piriformis Syndrome.
Actual Study Start Date :
Jan 11, 2020
Actual Primary Completion Date :
Sep 17, 2020
Actual Study Completion Date :
Sep 24, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Graston

Ultrasound, Graston technique, piriformis stretching, home plan (hip abductor and extensor strengthening)

Other: Graston
Ultrasound for 10 mins/1 set/ (3 sessions/week), Graston for 5 mins/1 set/ (3 sessions/week), Piriformis stretching exercises/ 10 reps with 30 sec hold/ 1 set/(3 sessions/week), Hip abductor strengthening/10 reps/1 set/(3 weeks), Hip extensor strengthening/10 reps/1 set/(3 weeks), A total of 9 sessions for 3 weeks (3 sessions/week) were given each consisting of 20 mins.

Active Comparator: Manual myofascial release

Ultrasound, Manual myofascial release, piriformis stretching, home plan (hip abductor and extensor strengthening)

Other: Manual myofascial release
Ultrasound for 10 mins/1 set/ (3 sessions/week), Manual myofascial release for 5 mins/1 set/ (3 sessions/week), Piriformis stretching exercises/ 10 reps with 30 sec hold/ 1 set/(3 sessions/week), Hip abductor strengthening/10 reps/1 set/(3 weeks), Hip extensor strengthening/10 reps/1 set/(3 weeks), A total of 9 sessions for 3 weeks (3 sessions/week) were given each consisting of 20 mins.

Outcome Measures

Primary Outcome Measures

  1. Numeric Pain Rating Scale [9th day]

    Changes from baseline and after 1st session, Numeric pain rating scale is a scale from 0 to 10. 0 indicating no pain and 10 indicating worse pain.

  2. Piriformis muscle length [9th day]

    Changes from baseline and after 1st session, in prone lying range of internal rotation is measured for piriformis muscle length

  3. Lower extremity functional scale [9th day]

    Changes from baseline and after 1st session, lower extremity functional scale is used to measure the functional status of patients with piriformis syndrome.

Secondary Outcome Measures

  1. Straight leg raise [9th day]

    Changes from baseline and after 1st session, goniometer is used to measure the straight leg raise range.

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 60 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No

Inclusion Criteria:•

  • Pain more than 1 month.

  • Piriformis syndrome diagnosed through screening test (FAIR test, Beatty test, Freiberg test, Sign of Pace)

Exclusion Criteria:
  • Leg pain due to causes other than piriformis syndrome.

  • Congenital spinal deformity.

  • History of fracture.

  • History of back or hip surgery.

  • Any systemic illness like metastatic or infective disorders.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Federal government polyclinic hospital Islamabad Fedral Pakistan 46000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Principal Investigator: Asghar Khan, Phd, Riphah International University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT04588779
Other Study ID Numbers:
  • REC/00689 Sonia Wali
First Posted:
Oct 19, 2020
Last Update Posted:
Oct 19, 2020
Last Verified:
Oct 1, 2020
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 Oct 19, 2020