Status:

COMPLETED

Expiratory Muscle Training in Patients With Parkinson's Disease

Lead Sponsor:

University of Florida

Conditions:

Parkinson's Disease

Eligibility:

All Genders

35-85 years

Phase:

PHASE1

PHASE2

Brief Summary

Respiratory difficulty is one of the primary factors leading to death in patients with Idiopathic Parkinson's Disease (IPD). The progressive degeneration of a family of segregated motor and non-motor ...

Eligibility Criteria

Inclusion

  • Adults between the age of 35 and 85 years.
  • Diagnosis of Idiopathic Parkinson's Disease (either tremor-predominant or rigid- predominant) by their neurologist.
  • Disability level of II, III, or IV (Hoehn \& Yahr, 1976) as indicated in their most recent neurological evaluation.
  • Forced Expiratory Volumes (FEV1) and forced vital capacity (FVC) within normative range for age and sex determined by a pulmonary function screening.
  • Persons who are able to maintain their current level of physical activity (including both aerobic exercise and weightlifting) throughout the entire training period.
  • \*Subjects will be asked to report any significant changes in their level of activity throughout their participation in the study in regards to intensity and frequency of exercise (i.e. a sedentary person begins exercising three to four days per week).
  • Completion of the informed consent to participate in the study.

Exclusion

  • Other neurological disorders
  • Positive history of any of the following conditions:
  • Gastrointestinal disease
  • Gastro-esophageal surgery
  • Head or neck cancer
  • History of breathing disorders or diseases (e.g., Asthma, chronic obstructive pulmonary disease (COPD)).
  • Untreated hypertension
  • Heart disease
  • History of smoking in the last five years
  • Failing the screening test of pulmonary functions (e.g., FEV1/FVC \< 75%)
  • Difficulty in complying with the training protocol due to neuropsychological dysfunction (e.g., severe depression).
  • Other illness that would prevent patient from completing the protocol.

Key Trial Info

Start Date :

January 1 2004

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2008

Estimated Enrollment :

90 Patients enrolled

Trial Details

Trial ID

NCT00843739

Start Date

January 1 2004

End Date

December 1 2008

Last Update

September 20 2011

Active Locations (1)

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1

University of Florida

Gainesville, Florida, United States, 32611