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The Digital Memory Notebook

Compensation Training to Improve Everyday Functioning of Older Adults With Mild Cognitive Impairment and Subjective Cognitive Complaints: The Digital Memory Notebook

Status
Enrolling by invitation
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04240665
Acronym
DMN
Enrollment
20
Registered
2020-01-27
Start date
2020-11-11
Completion date
2026-12-31
Last updated
2026-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Impairment, Prodromal Alzheimer's Disease, Subjective Cognitive Complaints

Brief summary

Compensatory aids (e.g., alarms, calendars) play an important supporting role when completing everyday tasks (e.g., appointments, medication management), and there is a growing body of scientific work suggesting that compensatory training improves daily functioning. However, traditional paper-based calendars and to-do-lists have limitations related to accumulation of information, difficulty retrieving information, and remembering to complete activities. Such limitations may be overcome using a digital format through organized digital files, search functions, and alarms. This pilot project proposes to train older adults at risk for cognitive decline to use the Digital Memory Notebook (DMN), a tablet-based application (app), to support everyday functioning. The primary goal is to obtain preliminary evidence that a 6-week, individual and group-based DMN training intervention results in demonstrable changes in target behaviors (e.g., goal-directed DMN use to support everyday activities) among older adults with mild cognitive impairment (MCI) and subjective cognitive complaints (SCC). Participants will complete a curriculum involving 2-hour weekly sessions for 6-weeks. Each week will cover a specific function of the DMN and will include standardized goal-setting and weekly homework targets. Following the 6-week intervention, participants will continue to use the DMN app for 4-weeks to evaluate stability. Participants will complete a questionnaire packet 1 week prior to the 6-week intervention, 1 week after the 6-week intervention, and 5 weeks following the 6-week intervention. MCI and SCC participants will complete separate 6-week individual or group interventions spaced two months apart at UCD.

Detailed description

The manualized curriculum will involve 2-hour weekly sessions for 6-weeks. The study personnel will administer all intervention sessions. Each week will cover a specific function of the Digital Memory Notebook (DMN) and will include standardized goal-setting and weekly homework targets. A research assistant will assess homework adherence using a standardized form and through data extracted from the DMN (e.g., number of alarms set). Mild cognitive impairment (MCI) and subjective cognitive complaints (SCC) participants will complete separate 6-week individual or group interventions. Following the 6-week intervention, participants will continue to use the DMN app for 4-weeks to evaluate stability. Participants will also be asked to complete questions about their medical background including history of traumatic brain injury or stroke, as well as any current medical conditions and questions regarding demographics including age, ethnicity, and education. Potential participants will be told that participating in the study will involve completing questionnaires at 3 different time points within 12 weeks (i.e.,week 1, week 8, week 12), identifying a knowledgeable informant who will also complete questionnaires, participating in a 6-week course to learn how to use the DMN and to support everyday functioning, and to continue to use the DMN for one month following the intervention. Information collected will be in the form of counts (e.g., number of alarms set) and number of minutes spent on the device. Specific content entered into the DMN will not be reviewed.

Interventions

BEHAVIORALDigital Memory Notebook (DMN) Application

Subjects will be taught to utilize the DMN application through 2-hour weekly sessions for 6-weeks.

Sponsors

University of California, Davis
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

All participants will complete a curriculum involving 2-hour weekly sessions for 6-weeks.

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of subjective cognitive complaints (SCC) or Mild Cognitive Impairment (MCI) * Adults at least 60 years of age (no upper age limit) * Fluent in English * Available informant (study partner) to complete surveys

Exclusion criteria

* Unable to consent * Pregnant women * Prisoners

Design outcomes

Primary

MeasureTime frameDescription
Real-time data extracted from the DMN ApplicationChange in number of entries assessed weekly from first weekly session through Week 6 weekly session and for 4 weeks after the completion of the last sessiondata that is automatically collected by DMN (Calendar entries, to-do list entries, alarms set, journal entries)

Secondary

MeasureTime frameDescription
Participant Questionnaire OutcomesWeek 1, Week 8, and Week 12Questionnaires each consisting of 41 or fewer items on a Likert scale

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORSarah Farias, PhD

University of California, Davis

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026