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Hamstring InjuryNCT04820699

Post Isometric Relaxation and Mulligan Bent Leg Raise on Hamstring Tightness in High School Students

A study testing post isometric relaxation and muligan bent leg raise and muligan bent leg raise in people with Hamstring Injury and Hamstring Tendon Injury, run by Riphah International University 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
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Trial summary

This project was a Randomized clinical trial conducted COMPARATIVE STUDY OF POST ISOMETRIC RELAXATION AND MULLIGAN BENT LEG RAISE ON HAMSTRING TIGHTNESS IN HIGH SCHOOL STUDENTS Read more about this study

Who is it for?
Ages 13 to 18 yearsHealthy volunteers can take part
Conditions the study is for
Hamstring Injury, Hamstring Tendon Injury
What is being tested?
post isometric relaxation and muligan bent leg raise and muligan bent leg raise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
28 participants
Where
1 sitePakistan
Study dates
15 Jan 2019to 15 Aug 2019
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 13 to 18 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • Asymptomatic Individuals of both gender, aged 13 to 18 years were evaluated for unilateral or bilateral Hamstring tightness. Those who were unable to reach more than 160 degree of knee extension with hip held at 90 degree of flexion, as measured with the thigh held at 90 degrees of hip flexion), unable to complete SLR and meet the criteria of finger to floor test
  • were included.

Who cannot join

  • Individuals were excluded who presented with previous injury of lower limb or pain duration of one year. Also any deformities related to spine, hip and knees or any neurological disorder or with history of lower limb fracture or surgery were also excluded.Subjects with hamstring tightness associated with muscle soreness or with Inflammatory condition that could affect motion were also exluded from the study

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Riphah IU

    Lahore, Punjab Province, 54000

Other trials in Pakistan

About this study

Official title: Comparative Study of Post Isometric Relaxation and Mulligan Bent Leg Raise on Hamstring Tightness in High School Students

This project was a Randomized clinical trial conducted COMPARATIVE STUDY OF POST ISOMETRIC RELAXATION AND MULLIGAN BENT LEG RAISE ON HAMSTRING TIGHTNESS IN HIGH SCHOOL STUDENTS

Read the detailed description

Non Probability Convenient sampling was done. Patients following eligibility criteria from high schools located in vicinity of Jhang district were considered. Sample size was calculated with Epitool calculator. 28 Participants were randomly allocated in two groups equally via convenient sampling method. Baseline assessment was done initially. Group A was given post isometric relaxation and Group B was given mulligan bent leg raise Duration of research was almost 6 months. All 28 involved subjects were given 12 treatment sessions over a six-week period, which consisted of 02 treatment sessions per week . Then tightness of hamstrings was assessed by AKET, SLR and FTF test. The baseline outcome measures consisted of pain assessment using Numeric rating scale (NPRS), knee joint goniometry in active knee extension test (AKET) and straight leg raise (SLR), modified finger to floor test (FTF) to assess the flexibility of hamstring muscles. . All participants were provided written informed consent prior to commencement of the procedures. Data was analyzed by using SPSS version 23.

Being tested
post isometric relaxation and muligan bent leg raise, muligan bent leg raise

What participants receive

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

  • post isometric relaxation and muligan bent leg raiseOther

    6 week intervention

  • muligan bent leg raiseOther

    muligan bent leg raise

Study groups in NCT04820699
Study groupRoleWhat they receive
post isometric relaxationExperimentalGroup A received Post isometric relaxation technique (MET).The participants performed isometric contractions using 20% of their strength, 5 second holds with 5 seconds rest time in between each contraction
Receives: Other: post isometric relaxation and muligan bent leg raise
mulligan bent leg raiseExperimentalGroup B: Mulligan bent leg raise technique. Isometric contraction of hamstring muscle for progressively five greater position of hip flexion; three pain-free repetitions with 5 second hold was performed by participants
Receives: Other: muligan bent leg raise

What is being measured

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

  1. NUMERIC PAIN RATING SCALE for pain

    0-10 Rating,0 means no pain and 10 severe pain

    Measured: 2 months

  2. Knee joint goniometry in active knee extension test (AKET)

    The 90/90 test, also known as the Active Knee Extension (AKE) Hamstring Flexibility Test, measures hamstring flexibility, particularly when the hip is flexed. purpose: to assess the range of active knee extension in a position of hip flexion, as required in running and kicking.

    Measured: 2 months

  3. straight leg raise (SLR) test

    If symptoms are primarily back pain, it is most likely the result of a disc herniation applying pressure on the anterior theca of the spinal cord, or the pathology causing the pressure is more central. "Back pain only" patients who have a disc prolapse have smaller, more central prolapses.[1] If pain is primarily in the leg, it is more likely that the pathology causing the pressure on neurological tissue(s) is more lateral.[1] Disc herniations or pathology causing pressure between the two extremes are more likely to cause pain in both areas.

    Measured: 2 months

  4. modified finger to floor test (FTF)

    If the FTF test is limited by pain, the location and pain score out of 10 should be should be documented. If the FTF test is 0cm or the patient is able to place their palms to the floor with no pain, 10 with maximum pain

    Measured: 2 months

Timeline

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

  1. First posted29 Mar 2021
  2. Study start15 Jan 2019
  3. Primary completion15 Jun 2019
  4. Study completion15 Aug 2019

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
28 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04820699
Sponsor's protocol ID
REC/Lhr/18/1008
Status last verified
May 2021
First submitted
26 Mar 2021
Last updated
11 May 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Kalanekar TA, Koley S. A Comparative Study of Mulligans Bent Leg Raise versus Muscle Energy Technique in Asymptomatic Individuals with Hamstring Tightness.

Questions about this trial

What is this clinical trial studying?

A study testing post isometric relaxation and muligan bent leg raise and muligan bent leg raise in people with Hamstring Injury and Hamstring Tendon Injury, run by Riphah International University 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 2 inclusion and 1 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 11 May 2021. 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?

NUMERIC PAIN RATING SCALE for pain (time frame: 2 months). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT04820699, which also lists 1 linked publication.

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 11 May 2021.

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