Working Memory Training in Patients with Mild Cognitive Impairment

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorSt. Joseph's Hospital and Medical Center, Phoenix

About this trial

The purpose of this study is to test whether a special memory training program, called CogMed, can help people with early memory problems. The Investigators want to see if this training improves memory and also helps reduce stress.

The Investigators also want to see if CogMed results in changes to a blood biomarker called p-Tau 217, which possibly indicate Alzheimer's disease (AD).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female outpatients ages ≥ 50 years;

Meet Mayo Clinic Criteria for MCI. (Patients with mild cognitive impairment)

Access to the internet through computer

A proficiency in speaking and reading English or having a family member who is proficient in reading and speaking English and is willing to serve as a translator.

Disqualifiers

Mini Mental State Exam (MMSE) score less than 19 or patients diagnosed with moderate or severe dementia by a clinician.

In the opinion of the investigator, participation would not be in the best interest of the subject.

Trial design

Design model

Parallel

Treatments tested in this trial

  • CogMed

    Other intervention

    CogMed which is a computerized working memory training program developed by Karolinska University.

Treatment groups

10 Participants
are divided into 2 treatment groups
Group A: Intervention GroupExperimental treatment 1 intervention
Group B: Control GroupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Working Memory as measured by the WAIS-IV Digit Span Forward/Backward

The Digit Span Forward/Backward is a subset of the Wechsler Adult Intelligence Scale (WAIS) that captures attention efficiency and working memory.

Time frame
Will be assessed at baseline and again at a 3-month follow-up following the intervention period.
2

Working Memory as measured by the TMT-B

The Trail Making Test (TMT) is a well-established test sensitive to impairment in multiple cognitive domains.

Time frame
Will be assessed at baseline and again at a 3-month follow-up following the intervention period.
3

Working Memory as measured by Category Fluency Test

The Category Fluency Test (CFT) was created to assess semantic fluency. It consists of asking the individual to name as many animals as possible in 60 s. Performance on CFT can be evaluated through several components, such as the number of correct words, clusters, switching, related words, and intrusion and perseveration errors.

Time frame
Will be assessed at baseline and again at a 3-month follow-up following the intervention period.

Secondary outcomes

1

Change in Blood biomarker

We do not expect a significant change in p-Tau 217 during the short-proposed study duration, however, we projected that we will successfully recruit 10 MCI patients (Intervention group = N 5; and control group (N=5) that will be willing to undergo blood draw for determination of p-Tau 217 level.

Time frame
Will be assessed at baseline and again at a 3-month follow-up following the intervention period.
2

Perceived Stress Scale (PSS) Score

The Perceived Stress Scale (PSS) is used for measuring the perception of stress. It is a measure of the degree to which situations in one's life are appraised as stressful. The scale also includes questions about current levels of experienced stress (Cohen et al, 1983).

Time frame
Will be assessed at baseline and again at a 3-month follow-up following the intervention period.
3

Brief Resilience Scale (BRS) Score

The Brief Resilience Scale (BRS) has 6 items and is a reliable means of assessing resilience as the ability to bounce back or recover from stress (Smith et al., 2008).

Time frame
Will be assessed at baseline and again at a 3-month follow-up following the intervention period.
4

Pittsburgh Sleep Quality Index (PSQI) Score

The Pittsburgh Sleep Quality Index (PSQI) is a self-rated questionnaire designed to measure sleep quality and disturbance over past month (Buysse et al.,1989).

Time frame
Will be assessed at baseline and again at a 3-month follow-up following the intervention period.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

St. Joseph's Hospital and Medical Center, Phoenix

Lead sponsor

Barrow Neurological Foundation

Collaborator

Barrow Neurological Institute

Collaborator