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Development of Therapeutic Intervention for Sleep in Alzheimer/Caregiver Dyads (BEST-Sleep)

Yale University logo

Yale University

Status

Withdrawn

Conditions

Alzheimer's Disease

Study type

Observational

Funder types

Other

Identifiers

NCT02506374
1412015088

Details and patient eligibility

About

This non-intervention qualitative study will use focus groups to assess the feasibility and acceptability of a proposed intervention for a future study. The focus group will discuss a potential biobehavioral family self-management intervention designed to improve sleep in persons with Alzheimer's disease (PAD) and their caregivers (CG).

Full description

Approximately 16 caregivers of home-based PAD/CG dyads (person with Alzheimer's disease/caregiver dyads) will be recruited from the community. A series of two audiotaped focus groups will be conducted with these caregiver participants. The first focus group will explore perspectives on what constitutes a feasible and acceptable intervention to improve their sleep and associated symptoms. The second focus group will consist of follow up and confirmation of findings from the first focus group. The intervention will be developed and refined based upon focus group findings.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. screen positive on the PROMIS sleep disturbance and associated symptoms measures
  2. be a caregiver within a PAD/CG dyad
  3. speak/understand English
  4. agree to be audiotaped during focus group participation
  5. be at least 18 years of age

Exclusion:

  1. they negative on the PROMIS sleep disturbance and associated symptoms measures,
  2. are not a caregiver within a PAD/CG dyad,
  3. do not speak/understand English,
  4. refuse to take part in audiotaping of the focus groups,
  5. are not at least 18 years of age.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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