MedPath

to see effectiveness of the two various technique on hamsting length of the participants

Not Applicable
Registration Number
CTRI/2024/07/071676
Lead Sponsor
nil
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Normal asymptomatic subjects with no symptoms of hamstring tightness

Both male and female subjects

Age group 18years and above with limited SLR ROM less than 75 degrees

Exclusion Criteria

Low back pain

History of hamstring injury in past years

History of neurological disease or peripheral neuropathy

History of Orthopedic disorder affecting lower limb (e.g. femoral fracture, meniscal injury etc.)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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