Efficacy of continuous passive motion device in the shoulder joint stiffness

Randomized controlled trial to study of efficacy of continuous passive motion device on pain and range of motion in order to improve function, in the patients with shoulder joint stiffness

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20170719035173N2

Enrollment

Registered

2018-01-23

Start date

2017-07-23

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Frozen Shoulder. Adhesive capsulitis of shoulder

Interventions

Intervention 1: Intervention: conservative treatment and CPM device. Intervention 2: Control group: conservative treatment.

Rehabilitation

Intervention: conservative treatment and CPM device

Control group: conservative treatment

Eligibility

Sex/Gender

All

Age

40 Years to 65 Years

Inclusion criteria

Inclusion criteria: Diagnosis of shoulder joint stiffness Symptoms of stage 2 of disease Expired at least 3 months from the onset of the disease Age between 40-65

Exclusion criteria

Exclusion criteria: Herniation of cervical disks Joint shoulder stiffness due to neurological disease Injury during the study

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: At the initial of the threatment, 4, 6 Weeks. Method of measurement: Visual Analog Scale.	—

Secondary

Measure	Time frame
Shoulder range of motion. Timepoint: The initial of the threatment, 4, 6 weeks. Method of measurement: Goniometery.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamideh Azizi

University of Social Welfare and Rehabilitation Sciences

Ha.azizi@uswr.ac.ir+98 21 2218 0037

Outcome results

None listed

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