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Clinical Trials/NCT05887063
NCT05887063
Completed
Not Applicable

Investigating the Feasibility, Acceptability, and Impact of an Online UK Dementia Awareness Course for Informal Caregivers: A Mixed Methods Study

University College, London1 site in 1 country51 target enrollmentJune 13, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dementia
Sponsor
University College, London
Enrollment
51
Locations
1
Primary Endpoint
Percentage of target sample recruited within 6 months.
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to investigate whether an online Dementia Awareness Course is feasible for delivery and acceptable to informal caregivers of people living with dementia in the UK. It will also explore the impact of the course on different caregiver outcomes.

Detailed Description

All participants were given information on the study before providing informed consent. The participants were screened against eligibility criteria before being randomly allocated to either the treatment condition of attending the course, or the control condition of treatment as usual. Participants completed 5 outcome measures and a demographics questionnaire at baseline. The treatment group then attended a one-off half-day Dementia Awareness Course online, delivered by one trainee clinical psychologist. A month later, all participants completed the same 5 outcome measures and those who attended the course also attended a one-to-one half an hour online semi-structured interview.

Registry
clinicaltrials.gov
Start Date
June 13, 2022
End Date
December 6, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Self-identified informal caregiver of a person living with dementia in the community.
  • Residing in the U.K.
  • Ability to engage in a course delivered in English
  • Have access to an internet-connected device capable of videoconferencing (camera and microphone functioning)
  • Available to attend pre-specified dates for DAC-UK delivery.

Exclusion Criteria

  • Person living with dementia residing in residential care
  • Professional caregiver of people living with dementia.

Outcomes

Primary Outcomes

Percentage of target sample recruited within 6 months.

Time Frame: 6 months

Feasibility of recruitment, considered feasible if full sample successfully recruited within 6 month time frame

Percentage of participants retained at follow-up to measure feasibility of the study design.

Time Frame: 1 month

75% considered indicative of a feasible study design

Percentage of completion of outcome measures to measure feasibility and acceptability.

Time Frame: Baseline and 1 month

75% considered indicative of feasible and acceptable outcome measures

Retention and attendance percentages to measure feasibility and acceptability of the intervention.

Time Frame: 1 month

60% considered indicative of feasible and acceptable intervention

Qualitative acceptability of the intervention, as measured by qualitative thematic analysis of participant interviews to capture themes regarding participant experience of the course.

Time Frame: 1 month

Exploratory thematic analysis

Secondary Outcomes

  • Change from baseline in the mean GAIN measure scores at one-month follow up(Baseline and 1 month)
  • Change from baseline in the mean approaches to dementia (ADQ-19) scores at one-month follow up(Baseline and 1 month)
  • Change from baseline in the mean Zarit burden inventory scores at one-month follow up(Baseline and 1 month)
  • Change from baseline in the mean Quality caregiver-patient relationship (QCPR) scores at one-month follow up(Baseline and 1 month)
  • Change from baseline in the mean short sense of competence (SSCQ) scores at one-month follow up(Baseline and 1 month)

Study Sites (1)

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