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Reminiscence, Anxiety and Early Alzheimer's Disease

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Emory University

Status

Withdrawn

Conditions

Alzheimer's Disease

Treatments

Behavioral: Simple Reminiscence (SR)
Behavioral: Attention Control (AC)

Study type

Interventional

Funder types

Other

Identifiers

NCT02319681
IRB00075912

Details and patient eligibility

About

This study seeks to establish the acceptability and evaluate the limited efficacy of Simple Reminiscence (SR), a home-delivered non-pharmacological intervention designed to relieve stress, improve affect, and prevent or quell disruptive or maladaptive behaviors in community-residing individuals diagnosed with early Alzheimer's disease (EAD). Unmanaged episodes of anxiety can be antecedents of maladaptive behaviors, including agitation, anger, and sometimes even violence.

SR is a dyadic strategy; both the person with EAD and the caregiver engaged the patient's memory to interrupt a current episode of anxiety.

Full description

Through the intervention, family caregivers are trained to collaborate with and guide patients to access positive memories as a way to manage or move past the anxiety that plagues individuals with EAD - often arising when confronted by common complex tasks they previously were able to perform.

During the project's first six months (phase 1), the investigators will develop a series of 4 video-vignettes illustrating dyads (including one member with EAD) managing a variety of anxiety provoking scenarios associated with EAD (e.g., trouble reconciling a checkbook) through the use of SR.

During the second phase of the project, a research assistant will administer SR at four home visits. The SR intervention has three components:

  1. A didactic component using the SR manual that the couple retains (15 minutes);
  2. Viewing one of the brief video-vignettes illustrating the application of reminiscence techniques (5 minutes; a different video-vignette will be viewed at each visit; and
  3. Facilitation of caregiver practice in applying the techniques, using a recent example of anxiety-linked experience of the person with EAD (10 minutes). The caregiver is encouraged to learn and practice the techniques in order to cue and coach the person with EAD in their use.

The attention control treatment, a Social Visit, is a 30-minute activity in which the person with EAD, the caregiver and the research assistant (RA) review and discuss the day's newspaper headlines. The RA will use communication techniques specifically designed to keep the conversation present focused.

Both members of the dyad will collect saliva to evaluate diurnal cortisol secretion.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Live in the community
  • Reside with a primary caregiver who must be willing to participate in all study activities (the primary caregiver must have a familial or marital relationship with the person with EAD of sufficient length to support reminiscence activity [i.e., an adult child, a long-term spouse or committed partner])
  • Have received a diagnosis of Early Alzheimer's Disease from a primary care provider
  • Achieve a score on the mini-mental state examination (MMSE) between 19 and 25

Exclusion criteria

  • Unable to give consent
  • MMSE score lower than 19 or greater than 25.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Simple Reminiscence (SR) caregiver
Experimental group
Description:
Subjects are caregivers for a persons with EAD and will be administered SR intervention and an attention control treatment four times
Treatment:
Behavioral: Attention Control (AC)
Behavioral: Simple Reminiscence (SR)
Simple Reminiscence (SR) EAD
Experimental group
Description:
Subjects are persons with EAD and will be administered SR intervention and an attention control treatment four times
Treatment:
Behavioral: Attention Control (AC)
Behavioral: Simple Reminiscence (SR)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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