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Patient-reported Adverse Events From Osteopathic Manipulative Treatment

NCT02386085 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1303

Last updated 2019-04-25

No results posted yet for this study

Summary

Currently, there is a significant deficiency in evidence regarding the safety of osteopathic manipulative treatments (OMT). To address this deficit, this study is designed to systematically evaluate the incidence and severity of OMT adverse events and examine the relationship of these adverse events to the technique(s) used and the body region(s) treated. The study is being conducted at the clinics of participating members of DO-Touch.NET, the only known practice-based research network (PBRN) focused on osteopathic manual medicine research. Eligible patients who receive OMT at one of the participating clinics will be asked to complete either a paper or online survey regarding any adverse events they experience within 1, 3, and 7 days following their treatment. Information regarding their diagnoses, which osteopathic techniques were used in their OMT, and which body regions were treated will be obtained from participant medical records. This data will be used to answer the following research questions:

1. What is the incidence of adverse events from osteopathic manipulative treatment?
2. What types of adverse events occur following osteopathic manipulative treatment?
3. Are there individual osteopathic techniques in particular body regions that have higher incidences of adverse events than other techniques or body regions?
4. Is the incidence of adverse events higher for some patient conditions than others?

Conditions

  • Osteopathic Manipulative Treatment

Interventions

PROCEDURE

Osteopathic manipulative treatment (OMT)

OMT will be provided as part of the patient's health care, prior to enrollment in the study. All participants would have received the same intervention (OMT) if they had not enrolled in the study.

Sponsors & Collaborators

  • American Academy of Osteopathy

    collaborator OTHER

  • A.T. Still Research Institute

    collaborator OTHER_GOV

  • DO-Touch.NET

    collaborator UNKNOWN

  • A.T. Still University of Health Sciences

    lead OTHER

Principal Investigators

  • Jane C Johnson, MA · A.T. Still University of Health Sciences

  • Brian F Degenhardt, DO · A.T. Still University of Health Sciences

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-02-28
Primary Completion
2017-08-31
Completion
2017-08-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02386085 on ClinicalTrials.gov