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Clinical Trials/NCT01818778
NCT01818778
Completed
Not Applicable

The Efficacy of Using Volunteers to Implement a Cognitive Stimulation Program in Two Long-Term Care Homes

Queen's University1 site in 1 country52 target enrollmentMay 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Impaired Cognition
Sponsor
Queen's University
Enrollment
52
Locations
1
Primary Endpoint
Test of Memory and Learning - Senior Edition (TOMAL-SE)
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Many volunteers visiting seniors make socially-based "friendly visits". This study investigated the efficacy of volunteers making visits focused on stimulating cognition. Participants were randomly assigned to either a "friendly visit" control group or a cognitive stimulation group. Seniors receiving stimulation visits made statistically significant improvement in memory abilities.

Detailed Description

Older adults who maintain their cognitive skills and abilities are able to live more independently than those whose skills have deteriorated. The costs (money, time, personnel) associated with providing cognitive stimulation programs to residents in long-term care homes often prohibit the delivery of these programs. The present study explored the efficacy of using volunteers to administer a stimulation program in two long-term care homes. The program focused on stimulating reasoning, attention, and memory abilities using uncomplicated, pen-and-paper exercises. Thirty-six resident participants and 16 volunteer participants were randomly assigned to one of two parallel groups, either the control or stimulation group. For eight weeks, three times each week, control group participants met for standard "friendly visits" (casual conversation between a resident and volunteer) and stimulation group participants met to work through a variety of exercises meant to stimulate the cognitive abilities of residents. Results were analyzed using a 2-way ANOVA and indicated statistically significant Group x Time interactions for Verbal Memory (F(1, 33) = 7.92, p = .008), Non-Verbal Memory (F(1, 33) = 6.8, p = .014), Learning (F(1, 33) = 5.27, p = .028), and Verbal Fluency (F (1, 33) = 5.56, p = .024). Volunteers completed a post-study questionnaire which indicated that the volunteers in the stimulation group found their skills-based interactions more stimulating for residents. Given this showing of improved resident abilities, it is reasonable to assert that the study does demonstrate that a volunteer-administered, cognitive stimulation program can provide measurable gains in the cognitive abilities of older adults. Further studies concerning the role of volunteers in the maintenance of the cognitive abilities of older adults are recommended.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
July 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. John Kirby

Ph.D.

Queen's University

Eligibility Criteria

Inclusion Criteria

  • 65 years and over
  • living in a long-term care home
  • normal or corrected visual and auditory acuity
  • English proficiency
  • not currently using de-stabilizing, psychotropic medication known to impair cognition
  • ability and willingness to actively listen to and accurately follow 2-step instructions for at least 20 consecutive minutes

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Test of Memory and Learning - Senior Edition (TOMAL-SE)

Time Frame: 10 weeks

The TOMAL-SE was designed specifically for seniors and provides a thorough assessment, without being fatiguing (Reynolds \& Vorees, 2012). The battery includes normative data for ages 55:0-89:11. It is a paper-based test and takes approximately 25-35 minutes to administer. It provides scores for the following indexes: Verbal Memory, Non-Verbal Memory, Delayed Memory, and Learning.

Secondary Outcomes

  • Wechsler Abbreviated Scale of Intelligence - Second Edition (WASI-II; Wechsler, 2011)(10 weeks)

Study Sites (1)

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