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Sleep Enhancement for Older Adults Living With Memory Loss And Their Care Partners (SLEEPMATE)

Emory University logo

Emory University

Status

Enrolling

Conditions

Sleep Disturbance
Dementia

Treatments

Behavioral: Cognitive Behavioral Therapy for Insomnia

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06250725
5K23AG070378-03 (U.S. NIH Grant/Contract)
STUDY00006711

Details and patient eligibility

About

The purpose of this study is to determine if a 6-week videoconference intervention to teach skills to improve sleep is practical, acceptable, and helpful to persons living with memory loss, cognitive impairment, and/or dementia and care partners, individually or together.

Full description

Disturbed sleep is stressful to persons living with dementia (PLwD) and their caregivers. It contributes to the earlier placement of the PLwD in nursing homes and increases the risk for many psychological and cognitive health issues and poor quality of life for both the PLwD and the caregivers. Given the potential harmful side effects of medications, non-medication alternatives, such as Cognitive Behavioral Therapy for Insomnia (CBTi), may be safer to improve disturbed sleep in this population. CBTi which includes stimulus control, sleep compression, relaxation, sleep hygiene, and cognitive restructuring, is effective and has durable and sustained effects on sleep outcomes over the long term. CBTi has improved sleep disturbances in PLwD and their caregivers, separately. Since disturbed sleep in the PLwD-caregiver dyad is bidirectional and interdependent, targeting the pair as a unit for intervention has the potential to lead to improved sleep and health outcomes for both persons.

There is no current published research on CBTi when the PLwD and their caregivers receive the intervention at the same time; as a result, the research team aims to examine the 1) feasibility and 2) preliminary efficacy of 6-week CBTi intervention for community-dwelling PLwD and their caregivers who are both experiencing sleep disturbances. PLwD-caregiver dyads will participate in videoconferencing sessions. In addition, semi-structured interviews will take place to examine the acceptability and satisfaction with the intervention.

Enrollment

80 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for the PLwCI:

  • Diagnosis of Alzheimer's Disease and Related Dementias (ADRD), or caregiver-reported probable or possible cognitive impairment or
  • Montreal Cognitive Assessment (MOCA) score between 12 and 24;
  • Had ≥1 sleep problem ≥3x/week on the Neuropsychiatric Inventory (NPI)-Nighttime Behavior Subscale;
  • Have an eligible caregiver;
  • Be able to participate in the intervention sessions

Inclusion Criteria for Caregivers:

  • ≥18 years old, co-residing with persons living with cognitive impairment (PLwCI);
  • Regularly assist the care recipient with ≥1 of 7 basic activities of daily living or
  • ≥1 of 7 Instrumental Activities of Daily Living for the past 6 months;
  • Have difficulty falling asleep or difficulty staying asleep for the last three months or
  • Have a Pittsburgh Sleep Quality Index (PSQI) of 5 or greater

Exclusion Criteria:

  • PLwCI: Moderate to severe cognitive impairment
  • Individuals who are not yet adults
  • Pregnant women
  • Prisoners
  • Individuals who are not able to clearly understand English.

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

80 participants in 1 patient group

Cognitive Behavioral Therapy for Insomnia (CBTi)
Experimental group
Description:
Participant dyads will receive CBTi via videoconferencing sessions
Treatment:
Behavioral: Cognitive Behavioral Therapy for Insomnia

Trial contacts and locations

1

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Central trial contact

Glenna S Brewster, PhD, RN, FNP

Data sourced from clinicaltrials.gov

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