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Clinical Trials/NCT05187572
NCT05187572
Completed
Not Applicable

Effectiveness of Reminiscence Therapy Versus Cognitive Stimulation in Older Adults With Cognitive Decline: a Quasi-experimental Pilot Study

Paulo Costa1 site in 1 country106 target enrollmentApril 20, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cognitive Decline
Sponsor
Paulo Costa
Enrollment
106
Locations
1
Primary Endpoint
Change in cognition (person with cognitive decline)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Although data suggest that non-pharmacologic therapies such as Reminiscence Therapy (RT) and Cognitive Stimulation (CS) can potentially maintain or reverse this trend, cognitive impairment can be a precursor to neurodegenerative processes. This study aimed to assess how an RT and a CS program affected cognition, depressive symptomatology, and quality of life (QoL) in older persons with cognitive decline who attended community support institutions in central Portugal. For seven weeks, a quasi-experimental study with two arms (RT and CS program) was conducted. The intervention was completed by 76 of the 109 older persons who were first screened (50 in the RT program, 26 in the CS program). In both groups, a pre- and post-intervention analysis revealed statistically significant differences in cognition, particularly in older adults' delayed recall ability.

Registry
clinicaltrials.gov
Start Date
April 20, 2017
End Date
June 6, 2017
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Paulo Costa
Responsible Party
Sponsor Investigator
Principal Investigator

Paulo Costa

Researcher

Escola Superior de Enfermagem de Coimbra

Eligibility Criteria

Inclusion Criteria

  • Ability to give informed consent before study commencement;
  • Ability to participate in group activities for a period between 45 to 60 minutes;
  • No pronounced impairment of their visual and auditory abilities;
  • Mild to moderate cognitive decline, assessed as a score equal to or below 20 points in the Six-Item Cognitive Impairment Test (6-CIT).

Exclusion Criteria

  • Unstable clinical condition;
  • Prescribed with cholinesterase inhibitors and/or antipsychotics during the study period.

Outcomes

Primary Outcomes

Change in cognition (person with cognitive decline)

Time Frame: 8 weeks post baseline

Measured using the Montreal Cognitive Assessment (MoCA). Scale scores vary between 0 and 30 points; higher scores correspond to a higher cognition level.

Change in depressive dymptomatology (person with cognitive decline)

Time Frame: 8 weeks post baseline

Measured using the 10-items Geriatric Depression Scale (GDS-10). Scale scores vary between 0 and 10 points; scores equal or above 2 points correspond to a screening diagnosis of depression.

Change in quality of life (person with cognitive decline)

Time Frame: Pre-intervention (baseline), 8 weeks post baseline

Measured using the World Health Organization Quality of Life - module for older adults (WHOQOL-OLD-8). Scale scores vary between 8 and 40 points; higher scores correspond to a higher level of quality of life.

Study Sites (1)

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