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Clinical Trials/NCT06197971
NCT06197971
Recruiting
Not Applicable

Comparative Effects of Instrument Assisted Soft Tissue Mobilization and Therapeutic Cupping on Hamstring Tightness Among Football Players

Riphah International University1 site in 1 country30 target enrollmentOctober 20, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Flexibility
Sponsor
Riphah International University
Enrollment
30
Locations
1
Primary Endpoint
Hamstring pain
Status
Recruiting
Last Updated
2 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
October 20, 2023
End Date
February 20, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Hamstring pain

Time Frame: pre 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 motion

Time Frame: pre and 6 weeks post interventional

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

Flexibility

Time Frame: pre and 6 weeks post interventional

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

Study Sites (1)

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