Development of Therapeutic Intervention for Sleep in Alzheimer/Caregiver Dyads

NCT ID: NCT02506374

Last Updated: 2016-01-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2014-11-30

Study Completion Date

2016-01-31

Brief Summary

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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).

Detailed Description

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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.

Conditions

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Alzheimer's Disease

Study Design

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Observational Model Type

COHORT

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Yale University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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LuAnn Etcher, PhD

Role: PRINCIPAL_INVESTIGATOR

Yale University

Locations

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Jewish Senior Services

Fairfield, Connecticut, United States

Site Status

Countries

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United States

Other Identifiers

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1412015088

Identifier Type: -

Identifier Source: org_study_id

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