Use of PNF and Tissue Flossing to Treat Hamstring Tightness in Young Female Students

NCT ID: NCT07178132

Last Updated: 2025-09-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-02

Study Completion Date

2024-04-15

Brief Summary

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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

Researchers will compare Tissue flossing to a PNF (Proprioceptive neuromuscular facilitation) to see which on is more effective.

Participant will:

1. be provided one technique either tissue flossing or PNF in first day
2. physiotherapist will immediately measure the the change in flexibility or knee motion

2\. another technique will be applied after 1 week 3. again change in flexibility and knee motion will be recorded

Detailed Description

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Conditions

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Hamstring Tightness Muscle Tightness

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Tissue Flossing Arm

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.

Group Type EXPERIMENTAL

tissue floss band

Intervention Type OTHER

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

PNF Hold-Relax Arm

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.

Group Type ACTIVE_COMPARATOR

Proprioceptive Neuromuscular Facilitation

Intervention Type OTHER

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

Interventions

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tissue floss band

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

Intervention Type OTHER

Proprioceptive Neuromuscular Facilitation

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

Intervention Type OTHER

Other Intervention Names

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Floss band

Eligibility Criteria

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Inclusion Criteria

* 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

Exclusion Criteria

* 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
Minimum Eligible Age

18 Years

Maximum Eligible Age

25 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Guru Nanak Dev University

OTHER

Sponsor Role collaborator

Sakshi Negi

OTHER

Sponsor Role lead

Responsible Party

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Sakshi Negi

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Manpreet Kaur, MPT

Role: STUDY_DIRECTOR

Guru Nanak Dev University

Locations

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Guru Nanak Dev University

Amritsar, Punjab, India

Site Status

Countries

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India

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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2250/HG

Identifier Type: -

Identifier Source: org_study_id

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