- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02774018
Life Satisfaction and Psychopathology in Institutionalized Elderly People
May 12, 2016 updated by: Daniel Seabra, Irmandade da Misericórdia de Albergaria-a-Velha
Life Satisfaction and Psychopathology in Institutionalized Elderly People: The Results of an Adapted Mindfulness-Based Stress Reduction Program
The present study attempted to test the benefits of a Mindfulness-Based Stress Reduction (MBSR) program in Portuguese institutionalized elderly people, as a way to improve life satisfaction and reduce psychopathology.
The sample included 12 institutionalized elderly people, with ages between 65 and 91 (M = 82.58
years; SD = 7.87), that filled several selfreport questionnaires and were assessed with Mini Mental State Examination.
Participants attended to an adapted Mindfulness-Based Stress Reduction program (KabatZinn,1994), with 48 sessions (16 weeks) and Participants were evaluated before and after the intervention.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
12
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
65 years to 95 years (Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- literacy
- age above 65 years
Exclusion Criteria:
- presence of cognitive or sensorial
- impairment
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: 12 institutionalized elderly people
Mindfulness-Based Stress Reduction program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in depression levels assessed with the GDS
Time Frame: Pre-test and Post-test (4 months later)
|
GDS; Geriatric Depression Scale; Greenberg et al., 2005
|
Pre-test and Post-test (4 months later)
|
Change in anxiety levels assessed with the DASS-21
Time Frame: Pre-test and Post-test (4 months later)
|
DASS-21; Depression Anxiety Stress Scale; Lovibond e Lovibond, 1995
|
Pre-test and Post-test (4 months later)
|
Change in experiential avoidance levels assessed with the AAQ-II
Time Frame: Pre-test and Post-test (4 months later)
|
AAQ-II; Acceptance and Action Questionnaire; Bond, Hayes, Baer, Carpenter, Guenole, Orcutt, Waltz e Zettle, 2011
|
Pre-test and Post-test (4 months later)
|
Change in subjective pain levels assessed with the Faces Scale
Time Frame: Pre-test and Post-test (4 months later)
|
Faces Scale; Wong et al., 2001
|
Pre-test and Post-test (4 months later)
|
Change in life satisfaction levels assessed with the SWLS
Time Frame: Pre-test and Post-test (4 months later)
|
SWLS; Satisfaction with Life Scale; Diener et al., 1985
|
Pre-test and Post-test (4 months later)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2015
Primary Completion (Actual)
October 1, 2015
Study Completion (Actual)
October 1, 2015
Study Registration Dates
First Submitted
April 18, 2016
First Submitted That Met QC Criteria
May 12, 2016
First Posted (Estimate)
May 16, 2016
Study Record Updates
Last Update Posted (Estimate)
May 16, 2016
Last Update Submitted That Met QC Criteria
May 12, 2016
Last Verified
May 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 01_PSI_MINDFULNESS
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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