NCT07178132

Brief Summary

The goal of this clinical trial is to learn tissue flossing and proprioceptive neuromuscular facilitation effect in treating hamstring muscle tightness. The main questions it aims to answer are:

  1. 1.which technique is more useful in giving instant relaxation of hamstring muscle
  2. 2.can these technique increase muscle flexibility and knee motion
  3. 3.be provided one technique either tissue flossing or PNF in first day
  4. 4.physiotherapist will immediately measure the the change in flexibility or knee motion

Trial Health

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2024

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 2, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 10, 2024

Completed
5 days until next milestone

Study Completion

Last participant's last visit for all outcomes

April 15, 2024

Completed
1.4 years until next milestone

First Submitted

Initial submission to the registry

September 10, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

September 17, 2025

Completed
Last Updated

September 24, 2025

Status Verified

September 1, 2025

Enrollment Period

2 months

First QC Date

September 10, 2025

Last Update Submit

September 19, 2025

Conditions

Keywords

tightnesstissue flossingproprioceptive neuromuscular facilitationHamstring tightnessflexibility

Outcome Measures

Primary Outcomes (4)

  • Active Knee Extension Test

    With the participant supine and the hip flexed to 90°, the participant actively extends the knee. A goniometer was used to records the knee extension angle. Three trials are performed and the mean is used for analysis.

    From enrollment to the end of treatment at 1 week

  • Passive Knee Extension Test

    With the participant supine and the hip flexed to 90°, the examiner passively extends the knee until the first onset of resistance. A goniometer is used to records the knee extension angle. Three trials are performed and the mean is used.

    From enrollment to the end of treatment at 1 week

  • Straight Leg Raise

    With the participant supine, the examiner passively raises the extended leg until resistance . A goniometer at the hip measures maximum hip flexion angle (degrees). Three trials are performed and the mean is used.

    From enrollment to the end of treatment at 1 week

  • Sit-and-Reach Test

    The participant sits with legs extended and reaches forward along a standard sit-and-reach box . After a warm-up, three trials are performed and the mean score (cm) is recorded.

    From enrollment to the end of treatment at 1 week

Study Arms (2)

Tissue Flossing Arm

EXPERIMENTAL

Application of tissue floss band to hamstring muscle at moderate tension for 2 minutes, followed by flexibility testing via AKET (Active Knee Extension Test), PKET (Passive Knee Extension Test), SLR (Straight Leg Raise), and Sit-and-Reach.

Other: tissue floss band

PNF Hold-Relax Arm

ACTIVE COMPARATOR

Standard PNF hold-relax stretching technique of hamstring, followed by flexibility testing via AKET (Active Knee Extension Test), PKET (Passive Knee Extension Test), SLR (Straight Leg Raise), and Sit-and-Reach.

Other: Proprioceptive Neuromuscular Facilitation

Interventions

Floss band is wrapped in thigh from distal to proximal for 2 minutes. during this period patient is asked to actively perform movement for 2 minute, after that the band is removed and repeated once more. Immediately followed by flexibility measurements

Also known as: Floss band
Tissue Flossing Arm

Proprioceptive Neuromuscular Facilitation (PNF) Stretching using the hold-relax method: participants perform an isometric contraction of the hamstring at the end of its stretch range , followed by relaxation and passive stretch, then flexibility assessed similarly

PNF Hold-Relax Arm

Eligibility Criteria

Age18 Years - 25 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsOnly female participants were eligible for inclusion in this study. The study focused on young women because sex-related differences in hamstring flexibility, joint range of motion, and neuromuscular properties have been reported in the literature. Restricting the sample to female students provided a more homogeneous group and reduced variability related to gender differences, thereby enhancing internal validity
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Female subjects were included in the study
  • Subjects with hamstring muscle tightness were included
  • Subjects between the age group of 18-25 years were included

You may not qualify if:

  • Male subjects
  • Subject who didn't fulfill the age criteria
  • Subject with hamstring tear or other knee ligament injury
  • Any history of lower limb surgery dating back a year
  • Subjects with Lower back pain or any neurological compromise in the lower limb
  • Any acute injury like a sprain, strain, and open wound
  • Subjects who had latex allergies
  • Subjects with venous thrombotic disease, heart disease, respiratory illness, and dermatitis, in their lower legs were excluded

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Guru Nanak Dev University

Amritsar, Punjab, India

Location

MeSH Terms

Interventions

Muscle Stretching Exercises

Intervention Hierarchy (Ancestors)

Exercise TherapyRehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsPhysical Therapy ModalitiesExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Manpreet Kaur, MPT

    Guru Nanak Dev University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 10, 2025

First Posted

September 17, 2025

Study Start

February 2, 2024

Primary Completion

April 10, 2024

Study Completion

April 15, 2024

Last Updated

September 24, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

I did not include individual participant data in ClinicalTrials.gov to protect participant privacy and confidentiality.

Locations