Clinical Trials Directory

Trials / Completed

CompletedNCT05129293

Improving Prospective Memory Via Telehealth

Improving Prospective Memory Via Telehealth: A Randomized Feasibility Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Trinity Health Of New England · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Up to 70% of persons with multiple sclerosis (PwMS) experience cognitive impairment, which can have a significant impact on several aspects of their daily lives. One cognitive domain that has been shown to impact daily functioning, but is understudied in MS, is prospective memory (PM). While there have been successful PM interventions in other clinical populations, to date there has not been a specific PM intervention for PwMS that has been tested in a clinical trial. The study will be a double-masked randomized feasibility trial, with 18 participants randomized to a PM intervention and 18 participants randomized to an active control (psychoeducation). Participants will meet with an interventionist twice a week for four weeks. Feasibility will be assessed via 1) recruitment, enrollment, and retention; 2) adherence to the treatment; 3) treatment credibility and expectancy; and 4) treatment satisfaction. A preliminary effect size (Cohen's d) will be computed for the group difference using participants' performance on the Memory for Intentions Test, which will be given at baseline (week 1) and post-treatment (week 6). Participants will also complete a battery of neuropsychological measures as part of their baseline and post-treatment assessments.

Conditions

Interventions

TypeNameDescription
BEHAVIORALProspective Memory InterventionCognitive remediation focusing on prospective memory
BEHAVIORALEducationalPsychoeducation

Timeline

Start date
2021-11-01
Primary completion
2023-06-05
Completion
2023-06-30
First posted
2021-11-22
Last updated
2024-10-18
Results posted
2024-10-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05129293. Inclusion in this directory is not an endorsement.