NCT07844135

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
6mo left

Started Oct 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

2 active sites

Status
not yet recruiting

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

Study Progress2%
Oct 2026Apr 2027

First Submitted

Initial submission to the registry

September 22, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 28, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

October 1, 2026

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2027

Last Updated

September 28, 2026

Status Verified

September 1, 2026

Enrollment Period

6 months

First QC Date

September 22, 2026

Last Update Submit

September 22, 2026

Conditions

Keywords

Stage II frozen shoulderSpencer's techniqueMulligan techniqueMobilization with MovementPainShoulder range of motionQuality of life

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

EXPERIMENTAL

Participants will receive Spencer's Muscle Energy Technique together with conventional physiotherapy three sessions per week for four weeks.

Other: Spencer's Muscle Energy Technique With Conventional Physiotherapy

Group B: Mulligan's Technique

ACTIVE COMPARATOR

Participants will receive Mulligan's Mobilization with Movement together with conventional physiotherapy three sessions per week for four weeks.

Other: Mulligan's Mobilization With Movement With Conventional Physiotherapy

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.

Also known as: Spencer's Technique
Group A: Spencer's Technique

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.

Also known as: Mulligan MWM
Group B: Mulligan's Technique

Eligibility Criteria

Age30 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

Ibn e Sina Hospital and Research Institute

Multan, Punjab Province, Pakistan

Location

MeSH Terms

Conditions

BursitisPain

Interventions

Movement

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Physiological PhenomenaMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Muhammad Naveed Babur

    Superior University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Muhammad Naveed Babur

CONTACT

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
Model Details: Participants will be randomized into two parallel intervention groups of 36 participants each using a chit-and-lottery method.
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

Locations