Use of PNF and Tissue Flossing to Treat Hamstring Tightness in Young Female Students
Tightness
Comparative Effects of Tissue Flossing and Proprioceptive Neuromuscular Facilitation on Hamstring Flexibility and Knee Range of Motion in Young Female Students
1 other identifier
interventional
60
1 country
1
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.which technique is more useful in giving instant relaxation of hamstring muscle
- 2.can these technique increase muscle flexibility and knee motion
- 3.be provided one technique either tissue flossing or PNF in first day
- 4.physiotherapist will immediately measure the the change in flexibility or knee motion
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Feb 2024
Shorter than P25 for not_applicable
1 active site
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
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 10, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 15, 2024
CompletedFirst Submitted
Initial submission to the registry
September 10, 2025
CompletedFirst Posted
Study publicly available on registry
September 17, 2025
CompletedSeptember 24, 2025
September 1, 2025
2 months
September 10, 2025
September 19, 2025
Conditions
Keywords
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
EXPERIMENTALApplication 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.
PNF Hold-Relax Arm
ACTIVE COMPARATORStandard 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.
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
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
Eligibility Criteria
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
- Sakshi Negilead
- Guru Nanak Dev Universitycollaborator
Study Sites (1)
Guru Nanak Dev University
Amritsar, Punjab, India
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Manpreet Kaur, MPT
Guru Nanak Dev University
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.