Effectiveness of a Dementia Anti-Stigma Intervention in Rural Kenya

ConditionDementia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAfrica Institute of Mental and Brain Health (AFRIMEB)

About this trial

Stigma underlies many health disparities in Kenya, and dementia-related stigma is no different. Preliminary evidence highlights the short-term benefits of a dementia anti-stigma intervention in Kenya. The study aims to ascertain the long-term effectiveness of a locally developed dementia anti stigma intervention in order to establish a community resource that will improve dementia understanding, reduce stigma and improve health behaviours.

In AIM 1, the investigators will assess what public stigma towards people with dementia and their carers looks like in Kenya, through a survey (600). Individual interviews with 20 members of the general public who completed the survey will be conducted to explore what stigmatizing beliefs are held and why they form. Triangulation techniques will then be used to integrate quantitative and qualitative data. Reflecting on AIM 1 findings, the investigators will engage 20 key stakeholders to refine an existing anti-stigma intervention, to better target culturally specific misconceptions and negative beliefs about dementia (AIM2). In AIM 3, the investigators will determine the effectiveness of the intervention among members of the general public (n=184), through a stepped wedge cluster randomized trial (SWT).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Residents of Mbooni Sub county

Aged 18 years and above

Able to speak the local language (Kamba)

Have capacity to consent

Disqualifiers

Non residents of Mbooni Sub county

Less than 18 years

Do not speak the local language

Have no capacity to consent

Trial design

Design model

Sequential

Treatments tested in this trial

  • Dementia anti stigma intervention

    Behavioral

    The intervention is a train-a-trainer programme contextually developed, for delivery (via demonstrations and role-plays) by lay providers such as community health workers. It includes four sessions that promote: (i) understanding of dementia, (ii) demystifying myths and misconceptions, (iii) empathetic connections using videos of people with dementia and carers (virtual social contact) and (iv) social inclusion through a case vignette and discussions. It is delivered bi-weekly in a group setting and each session ranges between 1.5 to 2 hours.

Treatment groups

184 Participants
are divided into 2 treatment groups
Group A: Control (Pre-Intervention Phase)No intervention 0 interventions
Group B: Post-Intervention PhaseOther 1 intervention

Trial outcomes

Primary outcomes

1

Change in Dementia attitudes (measured by the Dementia Attitudes Scale (DAS))

Dementia attitudes will be assessed using the Dementia Attitudes Scale (DAS), a validated tool that measures participants' comfort and perceptions when interacting with people with dementia. Scores on the DAS range from 20 to 140, with higher scores indicating more positive attitudes.

Time frame
Assessments will be collected at baseline during enrollment of participants, then every 3 months up until 6 months after switch points of the intervention.
2

Change in Dementia knowledge (measured by the Dementia Knowledge Assessment Scale (DKAS))

Dementia knowledge will be assessed using the Dementia Knowledge Assessment Scale (DKAS), which evaluates knowledge across domains such as causes, symptoms, risk factors, and care of people with dementia. Scores on the DKAS range from 0 to 50, with higher scores reflecting greater knowledge.

Time frame
Assessments will be collected at baseline during enrollment of participants, then every 3 months up until 6 months after switch points of the intervention.

Secondary outcomes

1

Intervention acceptability

Acceptability of the intervention will be assessed through self-reported responses where participants will be asked about their satisfaction, perceived usefulness, and willingness to continue or repeat participation in the dementia anti-stigma sessions. Outcomes will be reported as the proportion of participants indicating that they found the intervention acceptable and would be willing to continue or engage in similar sessions in the future.

Time frame
Immediately post-intervention (within 2 weeks after completion of the 4-session program).
2

Change in Dementia engagement (Behavior)

This will be assessed through self-reported responses where participants will be asked about their willingness to interact with, support, and include people with dementia in community life. Outcomes will be reported as the proportion of participants providing affirmative responses.

Time frame
From baseline during enrollment of participants, then every 3 months up until 6 months after switch points of the intervention.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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