Maitland Vs Mulligan Mobilization in Patients With Shoulder Pain
Effectiveness of Maitland Vs Mulligan Mobilization in Patient With Shoulder Pain
1 other identifier
interventional
46
1 country
1
Brief Summary
- To find the effect of the Maitland Mobilization versus Mulligans Mobilization on the pain of the patient suffering from Shoulder pain.
- To determine the effectiveness of Mulligans Mobilization versus Maitland Mobilization on the functional status of the patient suffering from shoulder pain.
- To determine the effectiveness of Mulligans Mobilization versus Maitland Mobilization on the psychological health status of that patient.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jul 2025
Shorter than P25 for not_applicable
1 active site
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
July 3, 2025
CompletedFirst Posted
Study publicly available on registry
July 14, 2025
CompletedStudy Start
First participant enrolled
July 15, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 3, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedFebruary 25, 2026
February 1, 2026
3 months
July 3, 2025
February 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Change in Shoulder Pain Intensity Measured by Numeric Pain Rating Scale (NPRS)
The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable") High test-retest reliability has been observed in both literate and illiterate patients with rheumatoid arthritis (r = 0.96 and 0.95, respectively) before and after medical consultation.
4 Weeks
Shoulder Disability Level Measured by DASH (Disability of the Arm Shoulder and Hand Questionnaire)
The Disabilities of the Arm, Shoulder and Hand (DASH) questionnaire is a 30-item questionnaire that looks at the ability of a patient to perform certain upper extremity activities.
4 Weeks
Psychological Status Measured by Beck Depression Inventory Score
The Beck Depression Inventory (BDI) is a 21-item questionnaire used to assess the severity of depressive symptoms. Scores range from 0 to 63, with higher scores indicating more severe symptoms. Interpretation of scores generally follows these guidelines: 0-13: minimal depression, 14-19: mild depression, 20-28: moderate depression, and 29-63: severe depression.
4 Weeks
Cognitive & Emotional Response to Pain Measured by Pain Catastrophic Scale
The Pain Catastrophizing Scale (PCS) is a 13-item self-report questionnaire that measures an individual's negative cognitive and emotional responses to pain.
4 Weeks
Study Arms (2)
Group A
EXPERIMENTALMaitland Mobilization Oscillatory Glides
Group B
EXPERIMENTALMulligan Mobilization with Movement (MWM)
Interventions
Hot pack for 15 minutes Ultrasound for 5 minutes Mobilization with Movement (MWM) Patient sitting with therapist posterolateral to him/her. Therapist places the Mulligan belt across the humeral head and to his waist. Patient movement (Flexion, extension, \& abduction respectively) combined with therapist-applied joint gliding (postero-lateral Glide) MWM will be performed. 3 sets of 10 reps per session (30 seconds rest between sets) (3 sessions per week for 4 weeks)
Hot pack for 15 minutes Ultrasound for 5 minutes Maitland Mobilization Oscillatory Glides inferiorly during normal abduction. Glenohumeral caudal glide mobilization was given at the rate of 2-3 glides per second for 30 seconds for each glide, 5 sets were given. (3 sessions per week for 4 weeks)
Eligibility Criteria
You may qualify if:
- Shoulder pain from last 3 months to 1 year, Male and Female patients will be included \& Age 20 years to 60 years.
You may not qualify if:
- Pain more than 1 year, Patients with certain shoulder structural deformities \& Patients with autoimmune disease.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Saidu Group of Teaching Hospital Mingora Swat
Swāt, KPK, 19200, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ayesha Sadiq, MSPT (OMPT)
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 3, 2025
First Posted
July 14, 2025
Study Start
July 15, 2025
Primary Completion
October 3, 2025
Study Completion
December 31, 2025
Last Updated
February 25, 2026
Record last verified: 2026-02