- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06074653
Effects of Mulligans BLR and CR on Hamstrings Flexibility in Office Workers
October 11, 2023 updated by: Riphah International University
Comparative Effects of Mulligan Bent Leg Raise and Contract Relax Technique on Hamstring Flexibility in Office Workers
The aim of this research is to compare the effect of mulligan bent leg raise and contract relax technique on hamstring flexibility in office workers with sedentary life styles.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Flexibility is regarded as a crucial component of typical biomechanical operation.
A tight hamstring increases the risk of frequent impairment to the associated musculature and bony structure.
Hamstring muscles are associated with lumbar spine, pelvic and lower limb movement disorders and have been connected to low back discomfort and abnormal gait pattern.
It has been observed that long sitting and sedentary life style is directly related to reduce the hamstrings flexibility, so the persons with tight hamstrings are more prone to develop musculoskeletal disorders if not addressed properly.
Previous research has shown that contract relaxation and Mulligan's bent leg are both useful for increasing hamstring flexibility.
But there hasn't been much research comparing the two methods, Mulligan bent leg lift and contract relax, for hamstring muscle stiffness in middle age office employees; instead, it was done in young people and athletes.
Hence, the aim of present work is to study and compare the effectiveness of contract relax and Mulligan bent leg raise in middle age office workers with long sitting hours having hamstring tightness
Study Type
Interventional
Enrollment (Estimated)
52
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Aruba Saeed, PHD*
- Phone Number: 03344399403
- Email: aruba.saeed@riphah.edu.pk
Study Contact Backup
- Name: Faiza Ashraf, TDPT
- Phone Number: 03327673643
- Email: dr.faiza1234@gmail.com
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Recruiting
- Bari Builders and IT path limited
-
Contact:
- Faiza Ashraf, TDPT
- Phone Number: 03327673643
- Email: dr.faiza1234@gmail.com
-
Principal Investigator:
- Amna Pervaiz, MS OMPT*
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Middle age men and women (30 to 45 years)
- Working/ sitting hours ≥ 36 hours per week.
- Real estate and IT office workers.
- Participant with positive Active Knee Extension Test: A lag of 20degrees is considered normal from full extension, anything less than 20degrees is considered as hamstrings tightness
Exclusion Criteria:
- History of knee and hip injury
- Neurological impairment
- Other orthopedic conditions i.e., hip fracture, THR, TKR etc
- Fracture of lower limb
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Experimental group A
Subjects will receive 8 sessions of Mulligan Bent Leg Raise technique on dominant side
|
Treatment session will be conducted for 2 days a week for 4 weeks consecutively.
In first week only 20 minutes session will be given to each group.
Home exercise plan is also given.Pre and post intervention measurements will be taken at 2nd and 4th week.
Both dominant and non-dominant legs will be checked
|
Experimental: Experimental group B
Subjects will receive 8 sessions of PNF Contract Relax technique on dominant side
|
Treatment session will be conducted for 2 days a week for 4 weeks consecutively.
In first week only 20 minutes session will be given to each group.
Home exercise plan is also given.
Pre and post intervention measurements will be taken at 2nd and 4th week.
Both dominant and non-dominant legs will be checked
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Active Knee Extension Test
Time Frame: 4 weeks
|
AKE test with goniometry will be used to evaluate hamstring tightness.
Goniometer was used to measure the popliteal angle.
When popliteal angle becomes greater than 20 degrees then it's considered as Hamstring tightness.
"change will be measured from baseline to 4 weeks"
|
4 weeks
|
Lower Extremity Functional Mobility Scale
Time Frame: 4 weeks
|
The Lower Extremity Functional Mobility Scale will tell us about activities done by a healthy individual using their lower limbs.
The test-retest reliability is excellent ranging between 0.855 and 0.99.
"Change will be measured from baseline to 4 weeks"
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Faiza Ashraf, TDPT, Riphah International University
- Principal Investigator: Amna Pervaiz, MS OMPT*, Riphah International University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 3, 2023
Primary Completion (Estimated)
April 1, 2024
Study Completion (Estimated)
April 1, 2024
Study Registration Dates
First Submitted
October 3, 2023
First Submitted That Met QC Criteria
October 3, 2023
First Posted (Actual)
October 10, 2023
Study Record Updates
Last Update Posted (Actual)
October 12, 2023
Last Update Submitted That Met QC Criteria
October 11, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- REC/0164Amna Pervaiz
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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