COMPLETED

Osteopathic Manual Treatment for Hemiplegic Shoulder Pain and Upper Extremity Function in Stroke Patients

Conditions

Hemiplegic Shoulder Pain Osteopathic Manipulative Treatment stroke Osteopathic Manual Treatment OMT

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study assesses the feasibility and safety of performing osteopathic manual treatment (OMT) for hemiplegic shoulder pain in stroke patients. This study's participants will be adults with a first-time stroke diagnosis in the past 5 years and shoulder pain on the same side affected by stroke. Eligible participants will be placed on study for approximately 6 weeks and given either OMT or a sham treatment each week.

Official Title

The Effects of Osteopathic Manual Treatment on Hemiplegic Shoulder Pain and Upper Extremity Function in Stroke Patients: A Pilot Study

Quick Facts

Study Start:2024-07-23

Study Completion:2025-11-10

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT06098508

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Patients must be at least 18 years or older to participate in the study * Presence of shoulder pain on the side of the body affected by stroke * Patients must have a diagnosis of a first-time stroke within the past 5 years * Stroke type must be subcortical, brainstem, and/or right-MCA stroke. Participants with multiple stroke types within the first-time diagnosis may be included	* Presence of an active systemic or localized infection requiring antibiotic therapy * Presence of fracture in the area being treated * Presence of open wound in the area being treated * Presence of rheumatoid arthritis * Presence of known active malignancy * Presence of shoulder pain on the affected side within 3 months prior to stroke * Patients with left-MCA stroke diagnosis who demonstrate the presence of aphasia based on the Mississippi Aphasia Screening Test (MAST) * Patients who demonstrate hemispatial visual neglect based on screening motor-free visual perception test (MFVPT) * Patients already receiving any type of manual therapy by a certified therapist through their standard-of-care treatment * Patients who do not wish to participate * Patients who are not fit as judged by the study team * Patients who lack the capacity to consent for enrollment in the study based on the University of California San Diego Brief Assessment of Capacity to Consent

Inclusion Criteria

Exclusion Criteria

* Patients must be at least 18 years or older to participate in the study
* Presence of shoulder pain on the side of the body affected by stroke
* Patients must have a diagnosis of a first-time stroke within the past 5 years
* Stroke type must be subcortical, brainstem, and/or right-MCA stroke. Participants with multiple stroke types within the first-time diagnosis may be included

* Presence of an active systemic or localized infection requiring antibiotic therapy
* Presence of fracture in the area being treated
* Presence of open wound in the area being treated
* Presence of rheumatoid arthritis
* Presence of known active malignancy
* Presence of shoulder pain on the affected side within 3 months prior to stroke
* Patients with left-MCA stroke diagnosis who demonstrate the presence of aphasia based on the Mississippi Aphasia Screening Test (MAST)
* Patients who demonstrate hemispatial visual neglect based on screening motor-free visual perception test (MFVPT)
* Patients already receiving any type of manual therapy by a certified therapist through their standard-of-care treatment
* Patients who do not wish to participate
* Patients who are not fit as judged by the study team
* Patients who lack the capacity to consent for enrollment in the study based on the University of California San Diego Brief Assessment of Capacity to Consent

Contacts and Locations

Principal Investigator

Ashley Mohan, DO

PRINCIPAL_INVESTIGATOR

University of Wisconsin, Madison

Study Locations (Sites)

UW Health University Ave Rehabilitation Clinic

Middleton, Wisconsin, 53562

United States

Collaborators and Investigators

Sponsor: University of Wisconsin, Madison

Ashley Mohan, DO, PRINCIPAL_INVESTIGATOR, University of Wisconsin, Madison

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-23

Study Completion Date2025-11-10

Study Record Updates

Study Start Date2024-07-23

Study Completion Date2025-11-10

Terms related to this study

Keywords Provided by Researchers

stroke
hemiplegic shoulder pain
Osteopathic Manual Treatment
OMT

Additional Relevant MeSH Terms

Hemiplegic Shoulder Pain
Osteopathic Manipulative Treatment