Dementia Clinical Trials

Find Dementia Clinical Trials Near You

Promoting Independence With Compensatory Cognitive Rehabilitation: A Pilot Clinical Trial for Early-Stage Alzheimer's Disease

Who is this study for? Patients with early-stage Alzheimer's disease
What treatments are being studied? Structured External Memory Aid Treatment
Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Alzheimer's disease (AD) is one of the leading causes of disability in older adults. Because pharmacological approaches do not seem to prevent or slow the disease, clinicians need non-pharmacological interventions that might help people with AD remain independent for as long as possible. This study aims to evaluate the effects of a new behavioral treatment, the Structured External Memory Aid Treatment (SEMAT), for adults with mild cognitive impairment (MCI) designed to promote independent living skills by explicitly teaching the use of strategies and tools to compensate for cognitive weaknesses. Aim 1: Evaluate the efficacy of the SEMAT for improving functional performance in a pilot randomized trial. Aim 2: Evaluate demographic, clinical, and neuropsychological predictors of treatment adherence. Aim 3: Develop and refine the SEMAT manual and other materials for training future interventionists.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Maximum Age: 90
Healthy Volunteers: f
View:

• 60-90 years of age

• English Speaking

• Functional Vision and Hearing to Complete Phone Screen

• not taking or stable ( \>2 months) on nootropic meds

• amnestic mild cognitive impairment from probable Alzheimer's disease

Locations
United States
Delaware
University of Delaware
RECRUITING
Newark
Time Frame
Start Date: 2022-02-01
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 65
Treatments
Experimental: Immediate Treatment Group
Participants will complete 7, 60-minute SEMAT sessions over 7 weeks with their group.
No_intervention: Delayed Treatment Control
Participants will not receive the intervention immediately. After 8 weeks, participants in this arm will complete the SEMAT. This is not a crossover design, because the treatment effects from those in the immediate treatment group can not be taken away.
Related Therapeutic Areas
Sponsors
Leads: University of Delaware

This content was sourced from clinicaltrials.gov

Similar Clinical Trials