NCT05732259

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Feb 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 6, 2023

Completed
1 day until next milestone

First Submitted

Initial submission to the registry

February 7, 2023

Completed
9 days until next milestone

First Posted

Study publicly available on registry

February 16, 2023

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 30, 2023

Completed
25 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 24, 2023

Completed
Last Updated

August 29, 2023

Status Verified

August 1, 2023

Enrollment Period

4 months

First QC Date

February 7, 2023

Last Update Submit

August 26, 2023

Conditions

Outcome Measures

Primary Outcomes (2)

  • Sit to Reach Test (Change is being assessed)

    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.

    Change from Baseline range of motion at day 4

  • Active knee extension test (Change is being assessed)

    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.

    Change from Baseline range of motion at day 4

Study Arms (2)

Percussion therapy group

ACTIVE COMPARATOR

Group A was given Conventional treatment along with percussion therapy with Theragun PRO (1750-2400 rpm). •Participants lying in prone position on the couch received 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

Manual Myofascial Release technique group

ACTIVE COMPARATOR

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

Other: Manual Myofascial Release technique

Interventions

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.

Percussion therapy group

Manual myofascial release technique for 90 sec continuous.

Manual Myofascial Release technique group

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • 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)

You may not qualify if:

  • Any history of Low back pain.
  • Any traumatic History of lower extremity.
  • Arthritis
  • Sprain or Strain

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sehat Medical Complex, Lahore

Lahore, Punjab Province, 55201, Pakistan

Location

Study Officials

  • Zaid Mughal, DPT

    University of Lahore

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Project Director

Study Record Dates

First Submitted

February 7, 2023

First Posted

February 16, 2023

Study Start

February 6, 2023

Primary Completion

May 30, 2023

Study Completion

June 24, 2023

Last Updated

August 29, 2023

Record last verified: 2023-08

Locations