NCT06074653

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 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

First Submitted

Initial submission to the registry

October 3, 2023

Completed
Same day until next milestone

Study Start

First participant enrolled

October 3, 2023

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 10, 2023

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 30, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2024

Completed
Last Updated

April 9, 2025

Status Verified

April 1, 2025

Enrollment Period

7 months

First QC Date

October 3, 2023

Last Update Submit

April 7, 2025

Conditions

Keywords

hamstring tightnesscontract relaxmulligan bent leg raiseoffice worker

Outcome Measures

Primary Outcomes (2)

  • Active Knee Extension Test

    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

    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

Study Arms (2)

Experimental group A

EXPERIMENTAL

Subjects will receive 8 sessions of Mulligan Bent Leg Raise technique on dominant side

Other: Mulligan Bent Leg Raise technique

Experimental group B

EXPERIMENTAL

Subjects will receive 8 sessions of PNF Contract Relax technique on dominant side

Other: PNF Contract Relax technique

Interventions

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 group A

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 group B

Eligibility Criteria

Age30 Years - 45 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

  • History of knee and hip injury
  • Neurological impairment
  • Other orthopedic conditions i.e., hip fracture, THR, TKR etc
  • Fracture of lower limb

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bari Builders and IT path limited

Lahore, Punjab Province, Pakistan

Location

Study Officials

  • Faiza Ashraf, TDPT

    Riphah International University

    PRINCIPAL INVESTIGATOR
  • Amna Pervaiz, MS OMPT*

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 3, 2023

First Posted

October 10, 2023

Study Start

October 3, 2023

Primary Completion

April 30, 2024

Study Completion

April 30, 2024

Last Updated

April 9, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations