Osteopathic Manipulative Treatment for Back Pain

NCT ID: NCT03892759

Last Updated: 2022-04-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

31 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-04-01

Study Completion Date

2022-03-04

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will investigate if Osteopathic Manipulative Treatment (OMT) is beneficial for patients presenting with back pain.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Low back pain is the most common cause of disability in people under age 45 and accounts for 20% of all physician visits. Osteopathic manual treatment (OMT) has been used to manage patients with acute and chronic back pain. These treatments are often reported as beneficial by patients.

This study will examine the effect on functional status, range of motion, quality of life, and pain with Osteopathic Manipulative Treatment (OMT). Baseline will be defined as someone who has never had OMT, chiropractic, or massage, or has not received such treatments in the last 90 days. Back pain will be specific to pain presenting in the lumbar or thoracic regions of the spine.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Back Pain Lumbar Pain Thoracic Pain Somatic Dysfunction Fascial Distortion

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Pre/post prospective one group pilot study
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Evaluation and Treatment

Subjects will be evaluated through inspection and palpation of the thoracic and lumbar spine, and other body regions as necessary. The provider will make a diagnosis of somatic dysfunction based off the TART (tissue texture change, asymmetry, restriction of motion, tenderness/pain) findings.

Group Type OTHER

Osteopathic Manipulative Therapy

Intervention Type OTHER

A set of hands-on techniques used by Osteopathic Physicians for the assessment and treatment of somatic dysfunction.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Osteopathic Manipulative Therapy

A set of hands-on techniques used by Osteopathic Physicians for the assessment and treatment of somatic dysfunction.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adult 18 years of age or older
* Back pain
* Able to arrange transportation and arrive to three study appointments.

Exclusion Criteria

* May not have had manual treatment (massage, chiropractic, or OMT) in the last 90 days
* May not have any labs or imaging for their back pain recommended by their physicians the subject has not yet completed
* May not have had back surgery in past 60 days
* May not be pregnant or have given birth in the last 30 days
* May not have be unable to tell a member of the study team their name, city they live in and the current year.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Pacific Northwest University of Health Sciences

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Crystal Martin

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Crystal Martin, DO

Role: PRINCIPAL_INVESTIGATOR

Assistant Professor of Osteopathic Principles and Practice

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Pacific Northwest University of Health Sciences

Yakima, Washington, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

2019-006

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Effects of OMT on Interoception
NCT02464475 COMPLETED NA
OMT & Intractable Singultus
NCT07149025 COMPLETED NA