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A Comparative Analysis of Mobilization with Movement and Class IV LASER Therapy on Disability and Quality of Life among Non- Diabetic Adults with Adhesive Capsulitis.

A Comparative Analysis of Mobilization with Movement and Class IV LASER Therapy on Pressure Pain Threshold, Disability and Quality of Life among Non-Diabetic Adults with Adhesive Capsulitis: A Prospective Experimental Design - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086918
Enrollment
84
Registered
2025-05-14
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: Movement with Mobilization: Movement with Mobilization will be given for 5 days a week for 4 weeks Control Intervention1: Class IV LASER Therapy: Class IV LASER Therapy will be given 5

Sponsors

Dr Mansi Jain
Lead Sponsor
Prof Aksh Chahal
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1)Subjects between 45-75 years 2)Male and Female Subjects 3)Non-Diabetic Adults 4)Patient with unilateral grade I and Grade II Adhesive Capsulitis 5)Diagnosed by physicians with Magnetic Resonance Imaging (MRI). 6)Severe shoulder pain since at least 3 months 7)Severity of pain higher than three out of ten on Numeric Pain Rating Scale 8)Patients with restricted range of passive shoulder flexion, abduction, external rotation, extension of shoulder to less than 50% of contralateral shoulder

Exclusion criteria

Exclusion criteria: 1)History of shoulder trauma 2)Glenohumeral osteoarthritis 3)Use of opioid medication 4)History of any recent lungs, breast or bypass surgery 5)Psychiatric or physical illness which make it difficult to complete the treatment. 6)History of neuromuscular disease 7)Skin allergy 8)Surgical history of shoulder and patients with tendon calcification

Design outcomes

Primary

MeasureTime frame
Numeric Pain Rating Scale(NPRS)Timepoint: It will be measured pre & post treatment i.e. at baseline and at 4th week.

Secondary

MeasureTime frame
Shoulder pain and Disability Index (SPADI) Range of Motion (ROM) Pain Pressure ThresholdTimepoint: These will be measure pre and post treatment i.e. before 1st week and after 4th week of the treatment.

Countries

India

Contacts

Public ContactProf Aksh Chahal

Galgotias University

drakshchahal@gmail.com9711774174

Outcome results

None listed

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