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Mulligan Mobilization With Movement Method in the Treatment of Shoulder Problems

Comparison of Conventional Therapy and Mulligan Mobilization With Movement Method in the Treatment of Shoulder Problems: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06187571
Enrollment
41
Registered
2024-01-02
Start date
2022-06-01
Completion date
2022-11-01
Last updated
2024-01-02

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

Conditions

Pain, Shoulder Syndrome

Brief summary

To determine whether Mulligan mobilization with movement (MWM) and Conservative treatment CT give different results on pain, ROM, and functional activities in participants with shoulder problems.

Detailed description

Shoulder problems are one of the common orthopedic problems. Patients with shoulder problems experience an increase in pain and a decrease in joint movement and functionality. With conventional treatment, patients' symptoms improve. However, the MWM is one of the manual therapy techniques frequently used to reduce pain in musculoskeletal system problems. It is extremely important to evaluate patients' functionality after rehabilitation. Although there are studies comparing the effect of MWM in the literature, studies evaluating patient-specific functionality are also limited.

Interventions

OTHERCT+MWM

The MWM technique was applied to the MWM group in addition to the CT. The MWM technique was applied in flexion, abduction, internal rotation, and external rotation directions. The MWM technique was performed with 3 sets of 10 repetitions.

OTHERCT

Cold packs, electrotherapy modalities, scapular mobilization, stretching, and strengthening exercises were applied to the CT group.

Sponsors

Ankara Yildirim Beyazıt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Being over 18 years old, * Having any shoulder problems (impingement, rotator cuff syndrome, glenohumeral joint problems, etc.), * Having a history of shoulder pain lasting at least 3 months, and volunteering to participate in the study.

Exclusion criteria

* Having systemic or degenerative disease, a neurological disease, and * Having more than one upper extremity pathology.

Design outcomes

Primary

MeasureTime frameDescription
Shoulder painthrough study completion, an average of 6 monthThe Numeric Pain Rating Scale was used to evaluate shoulder pain. The patient was asked to mark the point corresponding to the pain between 0 and 10. The higher the score, the higher the pain.

Secondary

MeasureTime frameDescription
ROMthrough study completion, an average of 6 monthShoulder flexion, abduction, internal and external rotation were measured using a Universal goniometer.As the angle increases, the joint range of motion increases.
Patient Specific Functional Scalethrough study completion, an average of 6 monthIn the patient-specific activity scale, depending on the current pathology, the physiotherapist asks the patient three or five activities that he or she finds difficult to do. The patient is asked to score the activity between 0-10 points. The total score is determined by averaging the activity scores, with higher scores indicating better function.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026