A Virtually Delivered Memory Rehabilitation Protocol in Older Adults

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

COMPLETED

Clinical Phase

NA

Total Enrollment

25 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-12-01

Study Completion Date

2021-12-20

Brief Summary

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The investigators conducted a feasibility study of a virtually-delivered adaptation of an ecologically oriented neurorehabilitation of memory (EON-Mem) in improving memory for healthy older adults. The primary purposes of this study included determining the feasibility of conducting EON-Mem virtually with older adults and whether a randomized control trial using EON-Mem in older adults is of value.

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Detailed Description

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Twenty-five older adults aged 55 years and older were recruited for participation in the EON-Mem training program adapted and administered virtually. Measures of emotional functioning and cognitive functioning were administered before and following the intervention. Participants attended one virtual treatment session per week for a total of six weeks with daily homework assignments. A priori, feasibility was set at an 80% completion rate. To address questions regarding feasibility, the investigators calculated descriptive statistics on sample information.

Conditions

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Memory Dysfunction Neurorehabilitation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

A feasibility study of twenty-five older adults completing the same virtual procedures.

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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Ecologically Oriented Neurorehabilitation of Memory (EON-Mem)

Feasibility study of a virtually-delivered adaptation of an ecologically oriented neurorehabilitation of memory (EON-Mem) in improving memory for healthy older adults

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Individuals 55 and older

Exclusion Criteria

* Evidence of cognitive dysfunction on the Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE) as evidenced by a score of 3.3 or more
* History of moderate-to-severe TBI
* History of stroke
* Dementia/neurological diagnoses
* Current chemotherapy or radiation
* Current or history of brain cancer
* Poor sensory function including uncorrected vision, hearing, or speaking impairments that could interfere with learning the intervention, including nonnative English speakers.

Minimum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes