MedPath

Effectiveness of supervised exercise on neck pain & functional disability

Phase 1
Registration Number
CTRI/2023/06/053945
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

Students who are using handheld devices more than 2 hours/day and having mild to moderate neck ache with mild and moderate functional disability

-Students who are between the age group of 18-24 years

-Subjects will be included in the study based on symptoms not by medical diagnosis

-Students who are having any two symptoms in the screening tool

Exclusion Criteria

- Those who already have severe neck pain

- Those with severe functional disability

- Those who are experiencing neck ache less than 1 week and more than 3 months

- Neck pain due to any other pathological or non-pathological causes including fall, injury, fractures and sprain etc

- Those who are on analgesics

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
After the intervention neck pain will be reducedTimepoint: 14 days
Secondary Outcome Measures
NameTimeMethod
After the intervention functional disability will be reducedTimepoint: 14 days
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