Use of Osteopathic Manipulative Treatment for Non-musculoskeletal Conditions

December 1, 2023 updated by: A.T. Still University of Health Sciences

Use of Osteopathic Manipulative Treatment for Non-Musculoskeletal Conditions: A DO-Touch.NET Card Study

The goal of this observational study is to learn how clinicians use osteopathic manipulative treatment (OMT) for their patients who have problems only related to their muscles, bones, and joints (ie, musculoskeletal problems) compared to patients whose problems involve other body systems (eg, infections, breathing, bowel function). The main questions it aims to answer are:

  • What percentage of patients receiving OMT have a non-musculoskeletal problem?
  • Is there a difference in the OMT techniques when the patient's problems include a non-musculoskeletal problem compared to patients with only musculoskeletal problems?

Surveys will be completed by the clinicians about 20 unique adult (age 18 or older) patients who have received OMT.

Study Overview

Status

Enrolling by invitation

Study Type

Observational

Enrollment (Estimated)

1000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Missouri
      • Kirksville, Missouri, United States, 63501
        • ATSU-KCOM OMM Clinic
        • Contact:

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.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adult patients receiving osteopathic manipulative treatment globally either in an outpatient or inpatient setting.

Description

Inclusion Criteria:

  • Adult patients receiving osteopathic manipulative treatment from a participating treatment provider

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Type of chief complaint
Time Frame: 24 hours
Multiple choice question: Do this patient's chief complaints include musculoskeletal complaints only, non-musculoskeletal complaints only, or both musculoskeletal and non-musculoskeletal complaints?
24 hours
Osteopathic manipulative treatment techniques
Time Frame: 24 hours
Multiple choice question (multiple answers): What OMT techniques did you use to treat this patient's somatic dysfunction? (list of 12 OMT technique categories)
24 hours

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Jane C Johnson, MA, A.T. Still University

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 Major Dates

Study Start (Actual)

December 1, 2023

Primary Completion (Estimated)

March 31, 2024

Study Completion (Estimated)

March 31, 2024

Study Registration Dates

First Submitted

September 13, 2023

First Submitted That Met QC Criteria

October 2, 2023

First Posted (Actual)

October 10, 2023

Study Record Updates

Last Update Posted (Actual)

December 5, 2023

Last Update Submitted That Met QC Criteria

December 1, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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