TY - JOUR
T1 - Multi-modal sleep intervention for community-dwelling people living with dementia and primary caregiver dyads with sleep disturbance
T2 - protocol of a single-arm feasibility trial
AU - Verma, Sumedha
AU - Varma, Prerna
AU - Brown, Aimee
AU - Bei, Bei
AU - Gibson, Rosemary
AU - Valenta, Tom
AU - Pietsch, Ann
AU - Cavuoto, Marina
AU - Woodward, Michael
AU - McCurry, Susan
AU - Jackson, Melinda L.
N1 - Funding Information:
This trial was funded by the Dementia Centre for Research Collaboration—Pilot Grant Scheme 2020. The development and delivery of focus groups was funded by an internal Turner Institute Sleep and Circadian Theme Consumer and Community Involvement Grant. The official trial sponsor is Monash University. The funding source and sponsor had no role in design of the current study and will have no role in undertaking of the trial, including data analyses, interpretation, or decision to submit results. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Funding Information:
The following grant information was disclosed by the authors: Dementia Centre for Research Collaboration—Pilot Grant Scheme 2020. An internal Turner Institute Sleep and Circadian Theme Consumer and Community Involvement Grant. Monash University.
Publisher Copyright:
© 2023 PeerJ Inc.. All rights reserved.
PY - 2023/12/14
Y1 - 2023/12/14
N2 - Background. Disturbed sleep is common among people living with dementia and their informal caregivers, and is associated with negative health outcomes. Dyadic, multi-modal interventions targeting caregiver and care-recipient sleep have been recommended yet remain limited. This protocol details the development of a singlearm feasibility trial of a multi-modal, therapist-led, six-week intervention targeting sleep disturbance in dyads of people living with dementia and their primary caregiver. Methods. We aim to recruit 24 co-residing, community-dwelling dyads of people living with dementia and their primary informal caregiver (n D 48) with sleep concerns (Pittsburgh Sleep Quality Index ≥5 for caregivers, and caregiver-endorsed sleep concerns for the person living with dementia). People who live in residential care settings, are employed in night shift work, or are diagnosed with current, severe mental health conditions or narcolepsy, will be excluded. Participants will wear an actigraph and complete sleep diaries for two weeks prior, and during the last two weeks, of active intervention. The intervention is therapist-led and includes a mix of weekly small group video sessions and personalised, dyadic sessions (up to 90 min each) over six weeks. Sessions are supported by a 37-page workbook offering strategies and spaces for reflections/notes. Primary feasibility outcomes are caregiver: session attendance, attrition, and self-reported project satisfaction. Secondary outcomes include dyadic self-reported and objectively-assessed sleep, depression and anxiety symptoms, quality of life, and social support. Self-report outcomes will be assessed at pre- and postintervention. Discussion. If feasible, this intervention could be tested in a larger randomised controlled trial to investigate its efficacy, and, upon further testing, may potentially represent a non-pharmacological approach to reduce sleep disturbance among people living with dementia and their caregivers.
AB - Background. Disturbed sleep is common among people living with dementia and their informal caregivers, and is associated with negative health outcomes. Dyadic, multi-modal interventions targeting caregiver and care-recipient sleep have been recommended yet remain limited. This protocol details the development of a singlearm feasibility trial of a multi-modal, therapist-led, six-week intervention targeting sleep disturbance in dyads of people living with dementia and their primary caregiver. Methods. We aim to recruit 24 co-residing, community-dwelling dyads of people living with dementia and their primary informal caregiver (n D 48) with sleep concerns (Pittsburgh Sleep Quality Index ≥5 for caregivers, and caregiver-endorsed sleep concerns for the person living with dementia). People who live in residential care settings, are employed in night shift work, or are diagnosed with current, severe mental health conditions or narcolepsy, will be excluded. Participants will wear an actigraph and complete sleep diaries for two weeks prior, and during the last two weeks, of active intervention. The intervention is therapist-led and includes a mix of weekly small group video sessions and personalised, dyadic sessions (up to 90 min each) over six weeks. Sessions are supported by a 37-page workbook offering strategies and spaces for reflections/notes. Primary feasibility outcomes are caregiver: session attendance, attrition, and self-reported project satisfaction. Secondary outcomes include dyadic self-reported and objectively-assessed sleep, depression and anxiety symptoms, quality of life, and social support. Self-report outcomes will be assessed at pre- and postintervention. Discussion. If feasible, this intervention could be tested in a larger randomised controlled trial to investigate its efficacy, and, upon further testing, may potentially represent a non-pharmacological approach to reduce sleep disturbance among people living with dementia and their caregivers.
KW - Caregivers
KW - Cognitive behavioural therapy
KW - Dementia
KW - Feasibility
KW - Insomnia
KW - Intervention
UR - http://www.scopus.com/inward/record.url?scp=85182211128&partnerID=8YFLogxK
U2 - 10.7717/peerj.16543
DO - 10.7717/peerj.16543
M3 - Article
AN - SCOPUS:85182211128
SN - 2167-8359
VL - 11
JO - PeerJ
JF - PeerJ
M1 - e16543
ER -