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Effect of kinesiotaping along with excercises in the management of pain, range of Motion and function in patients with frozen shoulder

Effectiveness of kinesiotaping as an adjunct to shoulder Rehabilitation protocol in the management of pain, range of Motion and function in patients with adhesive capsulitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/014304
Enrollment
30
Registered
2018-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- adhesive capsulitis

Interventions

Intervention1: Kinesiotaping group: The subjects will be initially treated with hot moist packs for 15 minutes. Taping done on day 1 and will be asked to remove on day 5 or as per needed, to be contin

Sponsors

sancheti institute college of physiotherapy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subject with primary adhesive capsulitis. 2. Patients with unilateral involvement. 3. Pain: VAS in the range of of 4-8 on 10 4. Range of motion (PROM less than or equal to a decrease in 50 % i.e 90 degrees of abduction and 45 degrees of external rotation as compared to normal)

Exclusion criteria

Exclusion criteria: 1. Operatively managed subjects. 2. Rotator cuff pathology. 3. Past Shoulder surgery in the last 1 year. 4. Patients with neurological deficits (eg. Stroke) 5. Patients having any cervical or thoracic problem 6. Cervical and thoracic spine dysfunction 7. Patients with polyarthritis, rheumatic disease or cervical radiculopathy 8. Patients undergone cardiac surgeries or other medical conditions like metastatic diseases. 9. Presence of shoulder dislocation or subluxation 10. Rib fracture or upper extremity fracture

Design outcomes

Primary

MeasureTime frame
1.)Visual analogue scale (VAS) for pain, 2.) shoulder range of motion 3.) shoulder pain and disability index (SPADI) for function.Timepoint: baseline and post intervention (10 days)

Secondary

MeasureTime frame
1.)Visual analogue scale (VAS) for pain, 2.) shoulder range of motion 3.) shoulder pain and disability index (SPADI) for function.Timepoint: baseline and post intervention (10 days)

Countries

India

Contacts

Public ContactPrachi Kadu
nilimabedekar@yahoo.com9420861882

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026