MedPath

Instrument Assisted Soft Tissue Mobilization vs Therapeutic Cupping on Hamstring Tightness Among Football Players

Not Applicable
Recruiting
Conditions
Range of Motion
Instrument Assisted Soft Tissue Mobilization
Flexibility
Hamstring Tightness
Registration Number
NCT06197971
Lead Sponsor
Riphah International University
Brief Summary

The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A \& B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive Instrument Assisted Soft Tissue Mobilization. Group B will receive Therapeutic Cupping.

Detailed Description

The objective of the study is to determine the effects of Instrument Assisted Soft Tissue Mobilization and Therapeutic Cupping on Hamstring tightness among football players. The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A \& B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive Instrument Assisted Soft Tissue Mobilization. Group B will receive Therapeutic Cupping. Players will be assessed by Numeric pain rating scale, Universal Goniometer and Sit \& Reach Test after the completion of treatment at 6 weeks.

The data will be analyzed by SPSS, version 25. Statistical significance is P=0.05.

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
30
Inclusion Criteria
  • Age (18-25),Male Gender Only,
  • Football Players, Bilateral Hamstring Tightness,
  • Previous hamstring injury in the last 6 months,
  • Positive SLR test,
  • Positive Passive/Active Knee Extension test
Exclusion Criteria
  • Malignancy of lower limb,
  • History of Lower Limb fracture in the last 6 months,
  • Post-surgical condition from past 6 months,
  • Neurological Conditions such as SLE, Herpes zoster, parkinsonism, Shingles disease, Musculoskeletal disorders like adductor tendinopathy, low back pain, knee injuries, hip injuries,
  • Skin Allergies.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Hamstring painpre and 6 weeks post interventional

Patient level of pain will be assessed by using Numerical Rating Scale (NRS) ranging from 0 to 10

Range of motionpre and 6 weeks post interventional

A goniometer is an instrument that measures the available range of motion at a joint.

Flexibilitypre and 6 weeks post interventional

The sit and reach test will be used to assess the flexibility of the hamstring muscles.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Pakistan sports board

🇵🇰

Lahore, Punjab, Pakistan

Pakistan sports board
🇵🇰Lahore, Punjab, Pakistan
Moiz Kamal, bachelors
Contact
0306-5595979
mkh.physio1@gmail.com
Sikander Naseer, DPT
Principal Investigator
Imran Ghafoor, M Phil
Sub Investigator

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