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Asthma and Osteopathic Manipulative Technique

The Effect of Osteopathic Manipulative Treatment on Respiratory Function in Patients With Asthma

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07071194
Enrollment
100
Registered
2025-07-17
Start date
2026-02-01
Completion date
2026-08-01
Last updated
2025-12-03

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

Conditions

Asthma

Keywords

Osteopathic Manipulative Treatment, Lung inflammation, Improved breathing

Brief summary

Asthma is a common respiratory condition that can be difficult to control despite the use of medications such as inhalers, oral steroids or even injectable medications. Osteopathic Manipulative Treatment (OMT) is a hands-on technique used to improve the chest structure and function and may help in improving breathing. Previous research showed that OMT in asthma patients, can improve the movement of the ribs and improve the peak flow which is the maximum rate at which a person can exhale air after taking a deep breath. However, no studies have evaluated the impact of OMT on lung inflammation. This single-site research study at University Hospitals aims to evaluate whether Osteopathic Manipulative Treatment (OMT) can reduce lung inflammation and improve breathing and lung function in adult patients with asthma. The lung function will be evaluated by Spirometry which is a test that measures how much air you can breathe in and out of your lungs, as well as how quickly and easily you can exhale air. The lung inflammation will be measured using a device that can detect how much you are breathing out Nitric Oxide which is a gas produced by inflamed cells in the lungs, this test is called: Fractional exhaled Nitric Oxide or FeNO. Approximately 100 participants will be enrolled.

Interventions

PROCEDUREOMT

Patients in the treatment group will undergo OMT using sub-occipital release, rib raising, doming the diaphragm, thoracic inlet release and myofascial techniques.

Patients in the control group will undergo light touch in similar locations to OMT.

Sponsors

University Hospitals Cleveland Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Male and female patients in Allergy and Immunology Associates clinic diagnosed with asthma ages 18-60 years old with an elevated FENO

Exclusion criteria

* Use of oral steroids within the last 4 weeks * Use of biologic medications * Diagnosis of pregnancy, osteoporosis, congestive heart failure, renal failure, cirrhosis, or cancer * Inability to lay recumbent

Design outcomes

Primary

MeasureTime frame
Change in Fractionated Exhaled Nitric Oxide (FeNO) values as measured by NIOX FeNO deviceBaseline, after OMT treatment (up to 30 minutes), day 10
Change in Peak Expiratory Flow values as measured by EasyOne Air Spirometer deviceBaseline, after OMT treatment (up to 30 minutes), day 10

Secondary

MeasureTime frameDescription
Change in Ease of breathing as measured by Post-OMT QuestionnaireBaseline and day 10The post\_OMT Questionnaire scores ease of breathing on a Likert scale of 1-0 with 1 being difficult to breathe and 10 being easy to breath
Change in Rib Cage mobility as measured by Post-OMT QuestionnaireBaseline and day 10The post\_OMT Questionnaire scores Rib Cage mobility on a Likert scale of 1-0 with 1 being stiff and 10 being mobile
Change in chest tightness as measured by Post-OMT QuestionnaireBaseline and day 10The post\_OMT Questionnaire scores chest tightness on a Likert scale of 1-0 with 1 being tight and 10 being loose

Countries

United States

Contacts

Primary ContactRemie Saab, MD
remie.saab@Uhhospitals.org(216) 381-3333

Outcome results

None listed

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