AzTrials
AzTrials

Hamstring SprainNCT05732259

Comparative Effect Of Percussive Therapy Device And Manual Myofascial Release Technique

A study testing Percussion therapy and Manual Myofascial Release technique in people with Hamstring Sprain, run by Sehat Medical Complex at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial 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… Read more about this study

Who is it for?
Ages 18 to 35 years, men onlyHealthy volunteers can take part
Conditions the study is for
Hamstring Sprain
What is being tested?
Percussion therapy and Manual Myofascial Release technique
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 sitePakistan
Study dates
6 Feb 2023to 24 Jun 2023
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • Men only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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)

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Sehat Medical Complex, Lahore

    Lahore, Punjab Province, 55201

Other trials in Pakistan

About this study

Official title: Comparative Effect Of Percussive Therapy Device And Manual Myofascial Release Technique To Improve Hamstrings Flexibility In Traffic Wardens

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.

Read the 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 was a Randomized clinical trial. Sample was taken through simple random sampling. Investigators will perform 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.

Being tested
Percussion therapy, Manual Myofascial Release technique

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Percussion therapyOther

    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.

  • Manual Myofascial Release techniqueOther

    Manual myofascial release technique for 90 sec continuous.

Study groups in NCT05732259
Study groupRoleWhat they receive
Percussion therapy groupActive comparatorGroup 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
Receives: Other: Percussion therapy
Manual Myofascial Release technique groupActive comparatorGroup B was given Conventional treatment along with manual myofascial release technique for 90 sec continuous.
Receives: Other: Manual Myofascial Release technique

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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.

    Measured: Change from Baseline range of motion at day 4

  2. 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.

    Measured: Change from Baseline range of motion at day 4

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Feb 2023
  2. Study start6 Feb 2023
  3. Primary completion30 May 2023
  4. Study completion24 Jun 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05732259
Sponsor's protocol ID
zaidmughal001
Status last verified
Aug 2023
First submitted
7 Feb 2023
Last updated
29 Aug 2023
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Percussion therapy and Manual Myofascial Release technique in people with Hamstring Sprain, run by Sehat Medical Complex at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 29 Aug 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Sit to Reach Test (Change is being assessed) (time frame: Change from Baseline range of motion at day 4). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Aug 2023.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in