Everyday Memory Intervention (EMMI)

April 3, 2024 updated by: Georgia Institute of Technology

Enhancing Older Adults' Everyday Memory Function

Evaluates an intervention designed to improve everyday memory function, contrasting people receiving the intervention with a group that receives traditional memory strategy training.

Study Overview

Detailed Description

This project seeks to develop and validate a novel approach to training everyday memory functioning in older adults. The approach (1) trains people to use simple but effective memory skills that have broad applicability in everyday life and (2) shapes a set of skills and habits of mind that will increase the likelihood of effective use of skills and memory aids. It is based on a metacognitive perspective on self-regulation in cognitively demanding situations and informed by recent theories about how suboptimal habit patterns can be altered. The approach has not yet been used in an everyday memory intervention in high-functioning, community-dwelling older adults. The proposed research validates ecological momentary assessment methods to get actual behavioral measures of forgetting in everyday life. It then uses these procedures in a randomized experiment that contrasts the everyday memory intervention group with a traditional memory-strategy training group. The hypothesis is that the everyday memory training intervention will reduce everyday memory errors and memory complaints, whereas the memory strategy training will alter strategy use and memory performance, with little cross-over effect. The hypothesized pattern will establish the explicit benefits of our everyday memory intervention procedures and demonstrate the limitation of standard memory training for that purpose.

Study Type

Interventional

Enrollment (Actual)

68

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Georgia
      • Atlanta, Georgia, United States, 30332
        • Adult Cognition Lab

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

70 years to 85 years (Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 70 - 85 years of age
  • in fair to good health
  • free of major neurocognitive impairment
  • English speaking
  • endorsed Smartphone and computer users (or willing to learn)

Exclusion Criteria:

  • diagnosis of any major neurological problems (e.g. stroke, Parkinson's disease, dementia)
  • 1.5 SD below age-normed mean (or lower) on the TICS
  • low computer and smart phone literacy
  • and poor self-rated health.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Everyday Metacognitive Memory
Training in techniques for managing memory demands in everyday life
Provides training in use of techniques and procedures to enhance proactive self-regulatory control over everyday memory demands, including strategies for learning information, planning for meeting everyday goals, and monitoring of efficacy of goal pursuit.
Active Comparator: Memory Strategy Control
Trains the use of memory strategies for learning new associations and concepts
Trains use of standard mnemonic techniques such as imagery and sentence generation for learning new associations and organizational and distinctiveness-based strategies for learning sets of items (e.g., word lists).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Everyday Memory Failures
Time Frame: minimum 8 day period after training on app prior to posttest
Across the data collection period, participants audio recorded descriptions of their memory failures on a smartphone app. The audio recordings were transcribed and then cleaned and qualitatively coded so that the number of memory failures each participant reported during the data collection period could be counted. The data was qualitatively coded to ensure an accurate count of the number of memory failures per participant without counting duplicate events or accidental reports. Average daily number of reported memory failures from EMA & daily diaries is reported.
minimum 8 day period after training on app prior to posttest
Prospective Memory Lab Contacts
Time Frame: Two weeks prior to posttest
Number of successfully completed lab contacts (maximum of 4)
Two weeks prior to posttest
Prospective Memory Lab Contact Efficiency
Time Frame: Two weeks prior to posttest
median absolute time deviation (in minutes) from scheduled lab contact for completed contacts
Two weeks prior to posttest
Everyday Cognition Simulation Task: ATM Task (Number of Errors)
Time Frame: posttest only
Computerized task to simulate use of an ATM machine. Measure: number of errors
posttest only
Czaja Everyday Cognition Simulation Task: Prescription Refill Task (Number of Errors)
Time Frame: posttest only
Computerized task to simulate use of an automated telephone program to refill prescriptions. Measure: Number of errors
posttest only
Free Recall Test
Time Frame: pretest and posttest (approximately 1 month lag)
Computerized task to present 30 concrete nouns, 6 from 5 taxonomic categories (Hultsch, Hertzog, Dixon, & Small, 1998) Measure is proportion of 30 words recalled
pretest and posttest (approximately 1 month lag)
Associative Recall Test
Time Frame: pretest and posttest (approximately 1 month lag)
Computerized task to present 40 concrete-concrete associatively unrelated noun pairs (Hertzog, Sinclair, & Dunlosky, 2010) Outcome is proportion of 40 words correctly recalled.
pretest and posttest (approximately 1 month lag)
Story Recall
Time Frame: posttest only
gist recall of narrative story (total number of propositions (ideas) from story recalled)
posttest only
Everyday Cognition Simulation Task: ATM Task (Time in Seconds)
Time Frame: posttest only
Computerized task to simulate use of an ATM machine. Measure: time to complete task (in seconds)
posttest only
Czaja Everyday Cognition Simulation Task: Prescription Refill Task (Time in Seconds)
Time Frame: posttest only
Computerized task to simulate use of an automated telephone program to refill prescriptions. Measure: time to complete task (in seconds)
posttest only

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
MFQ Memory Complaint (Frequency of Forgetting Scale)
Time Frame: pretest and posttest (approximately 1 month lag)
Summative Likert scale measuring frequency of reported memory problems for specific types of problems Measure is average item Likert rating on a 1-7 scale. Higher score indicates fewer memory problems
pretest and posttest (approximately 1 month lag)
PBMI Specific Memory Self-Efficacy
Time Frame: pretest and posttest (approximately 1 month lag)
The Personal Beliefs about Memory Instruments (PBMI) Specific Memory Self-Efficacy measurement is a summative visual analog rating scale measuring self-rated memory aggregated over multiple specific types of memory. Outcomes scaled in average proportion of distance from left (0) to maximum of 1.00 (higher scores indicate greater memory self-efficacy).
pretest and posttest (approximately 1 month lag)
PBMI Memory Control
Time Frame: pretest and posttest (approximately 1 month lag)
Summative visual analog rating scale measuring self-rated control over everyday. Outcome is scaled as average proportion of maximum endorsement (ranging from 0 to 1.0, with higher scores indicate greater perceived control)
pretest and posttest (approximately 1 month lag)
MCQ Internal Scale
Time Frame: pretest and posttest (approximately 1 month lag)
Summative Likert scale obtaining self-rated frequency of use of internal mnemonic strategies in everyday life. Average Likert rating on 1-5 scale (higher scores indicate greater use of strategies)
pretest and posttest (approximately 1 month lag)
MCQ External
Time Frame: pretest and posttest (approximately 1 month lag)
Summative Likert scale obtaining self-rated frequency of use of external memory aids. Outcome is scaled as average Likert rating on 1-5 scale. Higher score indicates greater use of external aids.
pretest and posttest (approximately 1 month lag)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Christopher Hertzog, Ph.D, Georgia Institute of Technology

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 15, 2021

Primary Completion (Actual)

December 10, 2021

Study Completion (Actual)

December 10, 2021

Study Registration Dates

First Submitted

September 11, 2019

First Submitted That Met QC Criteria

September 11, 2019

First Posted (Actual)

September 12, 2019

Study Record Updates

Last Update Posted (Actual)

May 1, 2024

Last Update Submitted That Met QC Criteria

April 3, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • H19341
  • 1R21AG059942-01A1 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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