Taping In Patients with Shoulder Impingement syndrome.

Not Applicable

Conditions: Health Condition 1: M754- Impingement syndrome of shoulder

Registration Number: CTRI/2020/05/024970

Lead Sponsor: DVVPFs College of Physiotherapy

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot Yet Recruiting

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1.Participants of both genders between age of 18- 65years.

2.Patients who had medically diagnosed with shoulder impingement syndrome or following clinical criteria of impingement in unilateral shoulder.

3.Clinical criteria include - onset of pain prior to 150-degree of shoulder elevation (flexion & abduction) and painful medial rotation, positive empty can test that define involvement of supraspinatus muscle and positive Hawkins-Kennedy test/ Neerâ??s sign indicating impingement syndrome.

4.Patient defined symptoms of anterior shoulder pain more than 2 month during overhead activity.

5.Shoulder Pain on NPRS ranging from 4-7.

Exclusion Criteria

1.Subjects with history of major trauma, shoulder fractures, dislocation and subluxation.

2.Patient underwent any surgical procedure for shoulder within the 12 weeks.

3.Patient had taken steroid injection over a period of 2 months.

4.Shoulder pain with cervical origin or cervical radiculopathy symptoms that effect the upper extremity.

5.Patients with rotator cuff calcification, adhesive capsulitis, post traumatic stiffness and osteoarthritis of shoulder joint.

6.Rheumatoid arthritis, Reiterâ??s syndrome like systemic disease.

7.Patients with neurological symptoms or further medical or psychiatric disorders.

8.Subjects having allergy or skin irritation to kinesio-taping.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Numerical pain rating scale (NPRS) <br/ ><br>2. Acromio-humeral distance using ultrasonography. <br/ ><br>3. Range of motion using goniometer. <br/ ><br>4. Shoulder pain and disability index (SPADI)Timepoint: Baseline, immediately post treatment, 3 days after intervention

Secondary Outcome Measures