A Structured Qi-gong Program for Hospitalized Older Adults

Sponsor
Fundacio Salut i Envelliment UAB (Other)
Overall Status
Completed
CT.gov ID
NCT00944788
Collaborator
(none)
58
1
2
2
28.5

Study Details

Study Description

Brief Summary

The purpose of this study is to test the effects on a number of health outcomes and the feasibility of a structured program of qi-gong, a form of tai-chi which has been previously tested in older populations, in older hospitalized patients. In particular, this pilot study aims to assess changes in quality of life and depressive symptoms after 4 weeks of treatment, with the hypothesis that this intervention will have a positive impact on these two domains, compared to usual care. Adherence will be also monitored in the intervention arm.

Condition or Disease Intervention/Treatment Phase
  • Other: qi-gong
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
58 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Feasibility and Impact on Quality of Life and Depressive Symptoms of a Structured Qi-gong Program for Hospitalized Older Adults. A Pilot Study.
Study Start Date :
Jul 1, 2009
Actual Primary Completion Date :
Sep 1, 2009
Actual Study Completion Date :
Sep 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: qi-gong

Other: qi-gong
Physical activity similar to tai-chi

No Intervention: Usual care

Outcome Measures

Primary Outcome Measures

  1. Quality of life [4 weeks]

Secondary Outcome Measures

  1. Depressive symptoms [4 weeks]

  2. Adherence [4 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • =50 years old

  • Preserved ability to move inside the house (also using walking aids or chair)

  • Estimation of at least one month of hospitalization (convalescence or rehabilitation)

  • Ability and willing to sign informed consent

Exclusion Criteria:
  • Moderate to severe cognitive impairment (SPMSQ >= 4)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Parc Sanitari Pere Virgili Barcelona Spain 08023

Sponsors and Collaborators

  • Fundacio Salut i Envelliment UAB

Investigators

  • Principal Investigator: Marco Inzitari, MD, PhD, Fundació Institut Català de l'Envelliment

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Fundacio Salut i Envelliment UAB
ClinicalTrials.gov Identifier:
NCT00944788
Other Study ID Numbers:
  • FICE09071
  • CEEAH_UAB_792H
First Posted:
Jul 23, 2009
Last Update Posted:
Jun 13, 2013
Last Verified:
Jun 1, 2013
Keywords provided by Fundacio Salut i Envelliment UAB
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 13, 2013