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Yoga Program in Respiratory Function
This study has been completed.
Sponsored by: Catholic University of Brasília
Information provided by: Catholic University of Brasília
ClinicalTrials.gov Identifier: NCT00768235
  Purpose

This study tested the hypothesis that yoga practice can improve respiratory function in the elderly.


Condition Intervention Phase
Elderly
Other: yoga practice
Phase I
Phase II

U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study
Official Title: Influence of Yoga Program in Respiratory Function of Older Women

Further study details as provided by Catholic University of Brasília:

Primary Outcome Measures:
  • Maximal inspiratory and expiratory pressure (IPmax and EPmax) were assessed by a manovacuometer and tidal volume (VT), vital capacity (VC) and minute ventilation (VE) were assessed by a ventilometer [ Time Frame: pre-intervention and post-intervention ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Maximal inspiratory and expiratory pressure (IPmax and EPmax) were assessed by a manovacuometer and tidal volume (VT), vital capacity (VC) and minute ventilation (VE) were assessed by a ventilometer [ Time Frame: pre-intervention and post-intervention ] [ Designated as safety issue: Yes ]

Enrollment: 36
Study Start Date: March 2007
Study Completion Date: June 2007
Primary Completion Date: March 2007 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: yoga group: Experimental
Yoga group
Other: yoga practice
The yoga program comprised 70 min sessions, 3 times/week during 12 weeks
2: control group: No Intervention

Detailed Description:

Maximal inspiratory and expiratory pressure (IPmax and EPmax) were assessed by a manovacuometer and tidal volume (VT), vital capacity (VC) and minute ventilation (VE) were assessed by a ventilometer. The yoga program comprised 70 min sessions, 3 times/week during 12 weeks.

  Eligibility

Ages Eligible for Study:   51 Years to 76 Years
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Sedentary women

Exclusion Criteria:

  • Physical impairment
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00768235

Locations
Brazil, Distrito Federal
Catholic university of brasilia
Brasilia, Distrito Federal, Brazil, 71966-700
Sponsors and Collaborators
Catholic University of Brasília
Investigators
Principal Investigator: Lidia MA Bezerra, Ms. catholic University of Brasilia
  More Information

article  This link exits the ClinicalTrials.gov site

Publications:
Responsible Party: ( Lidia Mara Aguiar Bezerra )
Study ID Numbers: UCByoga123, UCByoga12345
Study First Received: October 7, 2008
Last Updated: October 7, 2008
ClinicalTrials.gov Identifier: NCT00768235  
Health Authority: Brazil: Ethics Committee

Keywords provided by Catholic University of Brasília:
Sedentary elderly women that had medical assignment

ClinicalTrials.gov processed this record on January 15, 2009