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Observing the changes a wearable device creates on the movement of outward turning of the shoulder joint with clients having Frozen Shoulder.

Influence of external rotation splint on individuals with frozen shoulder

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/10/016203
Enrollment
39
Registered
2018-10-30
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: M750- Adhesive capsulitis of shoulder

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

School of Allied Health Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Limited external rotation range 2.Age range 30 years and above 3.Ending of stage 1 and complete stage 2 (in consultation with the orthopedic surgeon) 4.Patients referred for splint as a part of standard of care by the physician

Exclusion criteria

Exclusion criteria: 1.Secondary frozen shoulder 2.Associated injuries of the upper limb 3.Reflex sympathetic dystrophy (RSD) 4.Patients undergoing regular physical therapy 5.Osteoporotic changes

Design outcomes

Primary

MeasureTime frame
Flexilevel Scale of Shoulder Function (FLEX-SF) Goniometry of shoulder external rotationTimepoint: baseline at clients 1st visit—

Secondary

MeasureTime frame
Flexilevel Scale of Shoulder Function (FLEX-SF) Goniometry of shoulder external rotationTimepoint: 1 month after the 1st visit—

Countries

India

Contacts

Public ContactPaurvi Kedia

School of Allied Health Sciences, Manipal Academy of Higher Education

shovan.saha@manipal.edu9880059426

Outcome results

None listed

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