Effectiveness of Reminiscence Therapy Versus Cognitive Stimulation in Older Adults With Cognitive Decline

NCT05187572 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 106

Last updated 2022-01-12

No results posted yet for this study

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.

Conditions

Interventions

BEHAVIORAL

Group intervention

This intervention was developed during 14 sessions, held twice a week, with a duration of 45 to 60 minutes each. The sessions were developed as group-based interventions, facilitated by a leader and a co-leader from each community institution.

Sponsors & Collaborators

  • Junta de Freguesia de Santo António dos Olivais

    collaborator UNKNOWN
  • Centro Sociocultural Polivalente de São Martinho

    collaborator UNKNOWN
  • Centro Social e Paroquial de Carapinheira do Campo

    collaborator UNKNOWN
  • Obra Social de Torre de Vilela

    collaborator UNKNOWN
  • Centro Social Paroquial de Pedrulha

    collaborator UNKNOWN
  • Associação Nacional de Apoio ao Idoso

    collaborator UNKNOWN
  • Santa Casa de Misericórdia de Cantanhede

    collaborator UNKNOWN
  • Doce Viver - Residencial Sénior, Bruscos

    collaborator UNKNOWN
  • Paulo Costa

    lead OTHER

Principal Investigators

  • Rosa Silva, PhD · Health Sciences Research Unit: Nursing, Nursing School of Coimbra

  • João Apóstolo, PhD · Health Sciences Research Unit: Nursing, Nursing School of Coimbra

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-20
Primary Completion
2017-06-06
Completion
2017-06-06

Countries

  • Portugal

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05187572 on ClinicalTrials.gov