Comparative Effect Of Percussive Therapy Device And Manual Myofascial Release Technique

Sponsor
Sehat Medical Complex (Other)
Overall Status
Recruiting
CT.gov ID
NCT05732259
Collaborator
(none)
30
1
2
3.8
7.9

Study Details

Study Description

Brief Summary

The present study is concerned with the comparison of effect of Theragun PRO and manual myofascial release technique to improve Hamstrings Flexibility in healthy Adults. It will be randomized clinical trial on two groups one will get percussion therapy by theragun PRO and other will get treatment through manual myofascial release technique. The outcome measure will be hamstring flexibility.

Condition or Disease Intervention/Treatment Phase
  • Other: Percussion therapy
  • Other: Manual Myofascial Release technique
N/A

Detailed Description

Muscular flexibility is an important aspect of normal human function. Limited flexibility has been shown to predispose a person to reduce quality of life. Several studies developed protocols to improve flexibility of muscles, including manual myofascial release techniques, Stretching techniques or Percussive therapy. The studies about the effects of fascia relaxation and stretching techniques on flexibility reported that fascia relaxation increased flexibility of hamstrings. Many treatments likely combines the elements of a conventional massage and vibration therapy.

There is a lack of scientific evidence as to how and if percussive massage treatment affects ROM and muscle strength. To date, there are many studies on effect of percussive therapy on different muscle group, but investigators did not find work on hamstring muscle group. Therefore, it is aimed to find Comparative effect of Percussive therapy device and manual myofascial release technique to improve Hamstrings Flexibility in healthy Adults.

This would be a Randomized clinical trial. Sample would be taken through simple random sampling. Investigators will perform randomized clinical trial on two groups one will get percussion therapy by theragun PRO and other will get treatment through manual myofascial release technique. The outcome measure will be hamstring flexibility.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparative Effect Of Percussive Therapy Device And Manual Myofascial Release Technique To Improve Hamstrings Flexibility In Traffic Wardens
Actual Study Start Date :
Feb 6, 2023
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Percussion therapy group

Group A would be given Conventional treatment along with percussion therapy with Theragun PRO (1750-2400 rpm). •Participant lying in prone position on the couch will receive percussion therapy with Theragun PRO using standard ball head at speed of 1750 rpm, for total of 90 seconds, split into 3 sets of 30 seconds with 10 seconds rest

Other: Percussion therapy
Participant lying in prone position on the couch will receive percussion therapy with Theragun PRO using standard ball head at speed of 1750 rpm, for total of 90 seconds, split into 3 sets of 30 seconds with 10 seconds rest.

Active Comparator: Manual Myofascial Release technique group

Group B would be given Conventional treatment along with manual myofascial release technique for 90 sec continuous.

Other: Manual Myofascial Release technique
Manual myofascial release technique for 90 sec continuous.

Outcome Measures

Primary Outcome Measures

  1. Sit to Reach Test (Change is being assessed) [Change from Baseline range of motion at day 4]

    A yardstick is placed on the floor and tape is placed across it at a right angle to the 15 inches mark. The client/patient sits with the yardstick between the legs, with the legs extended at right angles to the taped line on the floor. Heels of the feet should touch the edge of the taped line and be about 10 to 12 inches apart. The score is the most distant point (cm or in) reached with the fingertips.

  2. Active knee extension test (Change is being assessed) [Change from Baseline range of motion at day 4]

    The subject is positioned on the examination table in supine, the lower limb that is'nt examined is positioned in stabilised on the support surface. The opposite limb is elevated so that the hip is in 90degrees of flexion and the knees are extended to reach a position perpendicular to the ground. A lag of 20degrees is considered normal from full extension, anything less than 20degrees is considered as hamstrings tightness. This range needs to be measure using a goniometer placed at the knee with the fulcrum at the lateral epicondyle, the stationary arm parallel to the thigh pointing to the greater trochanter and the moveable arm parallel to the leg pointing to the lateral malleoli.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18-35 years

  • Male gender

  • Traffic wardens with 5 years field experience

  • Participants labeled by Orthopedic surgeon/Physician with reduced flexibility of hamstring muscle group (Unilateral or Bilateral)

Exclusion Criteria:
  • Any history of Low back pain.

  • Any traumatic History of lower extremity.

  • Arthritis

  • Sprain or Strain

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sehat Medical Complex, Lahore Lahore Punjab Pakistan 55201

Sponsors and Collaborators

  • Sehat Medical Complex

Investigators

  • Principal Investigator: Zaid Mughal, DPT, University of Lahore

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Waseem Javaid, Project Director, Sehat Medical Complex
ClinicalTrials.gov Identifier:
NCT05732259
Other Study ID Numbers:
  • zaidmughal001
First Posted:
Feb 16, 2023
Last Update Posted:
Feb 17, 2023
Last Verified:
Feb 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Feb 17, 2023