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Role of Spencers technique in Reducing Pain and Improving Shoulder Function in Frozen Shoulder

Efficacy of Spencers technique on Pain, Range of Motion and Functional Disability among different stages of Frozen Shoulder patients - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/099992
Enrollment
45
Registered
2025-12-31
Start date
Unknown
Completion date
Unknown
Last updated
2026-01-12

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: Spencers technique effect in frozen shoulder patients: The Spencers technique intervention in Group 1(stages 1 )of frozen shoulder patients in between 35-70 year old for 6 weeks resear

Sponsors

Rashid
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Idiopathic frozen shoulder diagnosed with stage 1 2 or 3 Frozen shoulder characterized by unilaterally painful and stiff shoulder for at least three months Participants between the ages of 35 and 70 year Male or Female and diagnosed with adhesive capsulitis have shoulder pain and stiffness that started on their own and have limited active and passive ranges of motion for at least three months

Exclusion criteria

Exclusion criteria: Subjects with recent history of surgery on affected shoulder Rheumatoid arthritis Subjects with history of any trauma fracture around shoulder complex Osteoporosis and malignancies in shoulder region Neurological deficits affecting shoulder function Subjects with rotator cuff lesion and tendon calcification Pain or disorders of cervical spine elbow wrist or hand on affected side

Design outcomes

Primary

MeasureTime frame
Pain Range of Motion Timepoint: Pre intervention assessment(0 week) Post intervention assessment(3 weeks) Post intervention(6 weeks)

Secondary

MeasureTime frame
Functional disabilityTimepoint: Pre intervention assessment(0 week) Post intervention assessment(3 weeks) Post intervention(6 weeks)

Countries

India

Contacts

Public ContactDr Pragya Kumar

Amity University Noida

pkumar24@amity.edu9878529787

Outcome results

None listed

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