Skip to main content
OpenTrials
Completed

NCT Number: NCT02655497

Maintaining Independence in Everyday Life Among Seniors With Subjective Cognitive Complaints

The purpose of this study is to determine the effectiveness of cognitive strategies in improving participation in daily activities within older adults who report subjective cognitive decline.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Baycrest Health Sciences

Toronto, Ontario, M6A 2E1, Canada

About this study

The planned project explores the effects of several interventions designed to promote independence in everyday life, with older adults who identify cognitive complaints. Evidence suggests that 25-50% of community dwelling older adults report cognitive difficulties, such as reduced memory or concentration, in the absence of any diagnosed condition. Cognitive skills are crucial to living independently. The investigators plan to examine two approaches in a randomized controlled trial. Based on our successful pilot study, the investigators hypothesize that this training which combines education on healthy lifestyles and problem solving training to address everyday life difficulties, will be effective in maximizing and maintaining independence of older adults.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Community-dwelling older adults aged 60+
  • Fluent in written and spoken English
  • Have subjective cognitive complaints (SCC)
  • Performance within normal limits on a neuropsychological assessment battery
  • Participants must also be able to self-identify specific areas of difficulty in their everyday life that they would like to improve

Exclusion criteria

  • Significant neurological or psychiatric history (e.g., multiple sclerosis, psychiatric illness requiring hospitalization)
  • Concurrent depression
  • Anaesthesia in previous 6 months; and substance abuse

Treatment and study plan

Cognitive training

Behavioral

Psychosocial education

Behavioral

Primary outcomes

  1. Change in the Canadian Occupational Performance Measure (COPM) scores

    Time frame: 8 weeks after pretest and 3 months after intervention finished

    The Canadian Occupational Performance Measure (COPM) is the primary outcome measure. All participants will identify five everyday life activities that they need to or want to do using the COPM. The primary outcome will be (a) the number of goals improved by two points.

Sponsors and collaborators

Lead sponsor

Baycrest

Other

Collaborators

  • Canadian Institutes of Health Research (CIHR)

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Jan 14, 2016
Registry last updated
Nov 18, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.