Spencer's Technique Versus Mulligan's Technique for Stage II Frozen Shoulder
Comparative Efficacy of Spencer's Technique Versus Mulligan's Technique on Pain, Range of Motion, and Quality of Life in Patients With Stage II Frozen Shoulder
1 other identifier
interventional
72
1 country
2
Brief Summary
Stage II frozen shoulder (adhesive capsulitis) is associated with pain, stiffness, restricted shoulder range of motion, and reduced quality of life. This randomized controlled trial will compare Spencer's Muscle Energy Technique with Mulligan's Mobilization with Movement in adults with Stage II idiopathic frozen shoulder. Seventy-two participants will be randomized to two groups of 36. Both groups will receive their allocated manual therapy together with conventional physiotherapy for four weeks, three sessions per week. Outcomes will be assessed at baseline and after the 4-week intervention using the Numeric Pain Rating Scale, goniometric shoulder range of motion, and the SF-36 questionnaire.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2026
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 22, 2026
CompletedFirst Posted
Study publicly available on registry
September 28, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2027
September 28, 2026
September 1, 2026
6 months
September 22, 2026
September 22, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Pain Intensity Assessed by Numeric Pain Rating Scale (NPRS)
Pain intensity will be assessed using the 11-point Numeric Pain Rating Scale from 0 (no pain) to 10 (worst imaginable pain).
Baseline and immediately after the 4-week intervention
Shoulder Range of Motion Assessed by Goniometer
Shoulder flexion, abduction, and external rotation will be measured in degrees using a goniometer.
Baseline and immediately after the 4-week intervention
Health-Related Quality of Life Assessed by SF-36
Health-related quality of life will be assessed using the 36-item Short Form Health Survey (SF-36). Domain scores are transformed to a 0 to 100 scale, with higher scores indicating better health status.
Baseline and immediately after the 4-week intervention
Study Arms (2)
Group A: Spencer's Technique
EXPERIMENTALParticipants will receive Spencer's Muscle Energy Technique together with conventional physiotherapy three sessions per week for four weeks.
Group B: Mulligan's Technique
ACTIVE COMPARATORParticipants will receive Mulligan's Mobilization with Movement together with conventional physiotherapy three sessions per week for four weeks.
Interventions
Spencer's technique will use sequential passive shoulder movements including extension, flexion, circumduction with compression, circumduction with distraction, abduction, internal rotation, and external rotation. Conventional physiotherapy will include moist heat, shoulder isometrics, pulley and finger-ladder exercises, pectoral stretching, and Codman's pendulum exercises. Treatment will be provided three sessions per week for four weeks, approximately 30 to 40 minutes per session.
Mulligan's Mobilization with Movement will use a passive accessory glide applied in the direction of arm movement within the pain-free range. The protocol describes three sets of 10 repetitions with two minutes of rest between sets. Conventional physiotherapy will include moist heat, shoulder isometrics, pulley and finger-ladder exercises, pectoral stretching, and Codman's pendulum exercises. Treatment will be provided three sessions per week for four weeks, approximately 30 to 40 minutes per session.
Eligibility Criteria
You may qualify if:
- Male and female participants aged 30 to 55 years.
- History of idiopathic Stage II frozen shoulder.
- Experiencing shoulder pain for at least 3 months.
You may not qualify if:
- History of rotator cuff tears, rheumatoid arthritis, gouty arthritis, tumors of the shoulder region, or thoracic outlet syndrome.
- History of fracture of the upper limb involving the affected shoulder.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
City Hospital
Multan, Punjab Province, Pakistan
Ibn e Sina Hospital and Research Institute
Multan, Punjab Province, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Naveed Babur
Superior University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Single-blind design: the outcome assessor will be blinded to participant group allocation.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
September 22, 2026
First Posted
September 28, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
April 1, 2027
Study Completion (Estimated)
April 1, 2027
Last Updated
September 28, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share