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A Virtually Delivered Memory Rehabilitation Protocol in Older Adults (EONMem_OA)

B

Brigham Young University (BYU)

Status

Completed

Conditions

Memory Dysfunction
Neurorehabilitation

Treatments

Behavioral: Ecologically Oriented Neurorehabilitation of Memory (EON-Mem)

Study type

Interventional

Funder types

Other

Identifiers

NCT06187857
EONMem_OA

Details and patient eligibility

About

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.

Full description

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.

Enrollment

25 patients

Sex

All

Ages

55+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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