Promoting Reengagement in Daily Meaningful Activity Intervention for adults with mild cognitive impairment and their caregivers

  • End date
    May 31, 2024
Updated on 23 September 2022
Online studies
Accepts healthy volunteers


The PRIMA project is design to help persons with mild cognitive impairment to help them to improve their engagement in personally meaningful activity and improve their overall quality of life with their family caregivers support. The goal of PRIMA project is to increase persons with mild cognitive impairment’s engagement in meaningful activities, improve their physical and mental health, enhance communication between persons with mild cognitive impairment and their family caregivers (e.g. spouse, adult children, relative, or friend), and their overall quality life.


PRIMA (Promoting Reengagement in Meaningful Activity) Project: two group randomizations (DEMA Group vs. Information Support Group); a nurse intervener will each patient-caregivers will receive a total of 7 telephone sessions, bi-weekly for over 3 months. Each participant will complete 4-time outcome measures through telephone interview (baseline data, 2-weeks at post-program, 3 months at post-program, 6 and 9 months post-program). We expected the subjects will complete the project over 9 months.

Patients must: > 59 years of age , Speak English, Symptoms of memory loss or diagnosis of Mild Cognitive Impairment, Access to telephone, No hearing loss.  Caregivers (family member or friend) who self-identify as care partner ≥ 18 years of age, have primary responsibility for providing unpaid care/support to patients, along with providing social support, Be able to read and speak English, Be oriented to person, place, and time, Access to telephone

Condition Memory Loss, Mild Cognitive Impairment, MCI, Caregivers
Clinical Study IdentifierTX283461
Last Modified on23 September 2022


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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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