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

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

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.

Clinical Trials on Anxiety Depression (Mild or Not Persistent)

Clinical Trials on Mindfulness-Based Stress Reduction (MBSR) program

3
Subscribe