Use of PNF and Tissue Flossing to Treat Hamstring Tightness in Young Female Students
NCT ID: NCT07178132
Last Updated: 2025-09-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
60 participants
INTERVENTIONAL
2024-02-02
2024-04-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparative Effect Of Percussive Therapy Device And Manual Myofascial Release Technique
NCT05732259
Effectiveness Of The Application Of Percutaneous Electrolysis On Muscular Scar Tissue.
NCT06713200
Effects of Combining PNF With NMES in Young Basketball Players
NCT06648356
Stroking Versus Ergon Technique in Pregnant Women
NCT05665413
Effects of Pulsed Electromagnetic Field Therapy on Meniscal Healing, Symptom Relief, and Knee Function
NCT07117929
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
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.
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
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.
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
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
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
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
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Subjects with hamstring muscle tightness were included
* Subjects between the age group of 18-25 years were included
Exclusion Criteria
* 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
18 Years
25 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Guru Nanak Dev University
OTHER
Sakshi Negi
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Sakshi Negi
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Manpreet Kaur, MPT
Role: STUDY_DIRECTOR
Guru Nanak Dev University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Guru Nanak Dev University
Amritsar, Punjab, India
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2250/HG
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.