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Completed

NCT Number: NCT00258661

Is Osteopathic Manipulative Treatment (OMT) Beneficial for Elderly Patients Hospitalized With Pneumonia?

Osteopathic Manipulative Treatment (OMT) were used in the 1800s and 1900s to treat pneumonia before the introduction of antibiotics in the mid-1900s. The purpose of this study is to determine if OMT, when used in conjunction with antibiotics and other usual care, will improve the recovery of elderly pneumonia patients.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mount Clemens General Hospital, Mount Clemens, Michigan, United States

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About this study

This study is a multi-center study conducted across five sites in the United States to determine the efficacy of combining Osteopathic Manipulative Treatment(OMT)with antibiotics as a treatment regimen for elderly patients with pneumonia. The study is a prospective, randomized, controlled clinical trial, in which 360 subjects will be randomly assigned to three different groups to test the primary hypothesis that the combination of OMT and antibiotics will decrease the length of hospital stay for elderly patients with pneumonia. The first group (OMT Group) will receive a series of eight osteopathic manipulative techniques in combination with conventional antibiotic care. The second group (Light Touch Control Group) will receive a light touch mimic treatment in combination with conventional antibiotic care to control for the doctor-patient interaction. The third group (Conventional Care Only Group) will receive only the conventional antibiotic care normally given to elderly patients with pneumonia. The first two groups will receive two 15-20 minute treatments per day, at least six hours apart, for the duration of their stay in the acute care facility.

The primary outcomes for measuring efficacy are: Length of Hospital Stay, Time to Clinical Stability, and Rate of Symptomatic and Functional Recovery. The secondary outcomes are: duration of IV and oral antibiotic usage in the hospital, number of complications and deaths secondary to pneumonia, re-admission rate within 60 days of hospitalization admission date, duration and severity of fever, duration and severity of leukocytosis, and patient satisfaction.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 50 Years old or older
  • Subject is hospitalized in an acute care facility
  • Subject must exhibit at least two of the classic symptoms of pneumonia, to include:
  • Respiration Rate greater than or equal to 25 respirations per minute
  • New or increased cough
  • Fever greater than or equal to 100.4 degrees F (38 degrees C)
  • Pleuritic chest pain
  • Worsening of mental or functional status
  • Leukocytosis (WBC greater than 12,000 cells per cubic millimeter)
  • New or increased physical findings (rales, wheezing, bronchial breath sounds)

Exclusion criteria

  • Lung abscess
  • Advancing pulmonary fibrosis
  • Bronchiectasis
  • Pulmonary tuberculosis
  • Lung Cancer
  • Metastatic malignancy
  • Uncontrolled metabolic bone disease that places subject at risk for pathologic bone fracture (i.e. Paget's Disease or hypoparathyroidism)
  • Acute or unhealed rib or vertebral fracture
  • History of pathologic bone fracture
  • Previous participants as subject in the study
  • Respiratory failure (intubation)

Treatment and study plan

Osteopathic Manipulative Treatment

Procedure

In addition to conventional treatment for pneumonia, a 10-minute standardized OMT protocol + 5-minute nonstandardized component was performed twice daily for the duration of hospitalization.

Other names: OMT, OMM, Osteopathic Manipulative Medicine, Manipulation

Light-touch Treatment

Procedure

In addition to conventional treatment for pneumonia, a 10-minute standardized light-touch protocol (designed to mimic OMT standardized protocol) + 5-minute auscultation of carotid bruits, heart, and lungs was performed twice daily for the duration of hospitalization.

Other names: Sham manipulation, Placebo manipulation

Primary outcomes

  1. Length of Hospital Stay

    Time frame: End of hospital stay

    Number of days from admission order to discharge order

  2. Time to Clinical Stability

    Time frame: Daily for the duration of the hospital stay

    Halm EA, Fine MJ, Marrie TJ, Coley CM, Kapoor WN, Obrosky DS, et al.:

    Time to clinical stability in patients hospitalized with community-acquired pneumonia: implications for practice guidelines. JAMA 1998, 279:1452-1457

  3. Symptomatic and Functional Recovery Score

    Time frame: 14, 30, and 60 days post-admission

    Metlay JP, Fine MJ, Schulz R, Marrie TJ, Coley CM, Kapoor WN, et al.:

    Measuring symptomatic and functional recovery in patients with communityacquired pneumonia. J Gen Intern Med 1997, 12:423-430

Secondary outcomes

  1. Duration of IV and oral antibiotic usage in the hospital

  2. Number of complications and deaths secondary to pneumonia

  3. Duration and severity of fever

  4. Duration and severity of leukocytosis

  5. Patient Satisfaction

Sponsors and collaborators

Lead sponsor

A.T. Still University of Health Sciences

Other

Collaborators

  • Brentwood Foundation
  • Colorado Springs Osteopathic Foundation
  • Foundation for Osteopathic Health Services (Maryland)
  • Muskegon General Osteopathic Foundation (Michigan)
  • Northwest Oklahoma Osteopathic Foundation (Oklahoma)
  • Osteopathic Founders Foundation (Oklahoma)
  • Osteopathic Heritage Foundations
  • Osteopathic Institute of the South (Georgia)
  • Quad City Osteopathic Foundation (Iowa)

Registry information

Official study title

Multicenter Osteopathic Pneumonia Study in the Elderly (MOPSE)

Acronym: MOPSE

Important dates

Study start
2004
Primary completion
2007
Study completion
2007
First posted
Nov 28, 2005
Registry last updated
Oct 4, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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