Implementation of Cognitive Stimulation Therapy

NCT ID: NCT04754932

Last Updated: 2023-04-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

23 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-27

Study Completion Date

2022-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This project aims to examine the feasibility of implementing Cognitive Stimulation Therapy (CST) under real world circumstances in a more heterogenous population, with the ultimate goal of making the treatment broadly accessible. The effects of CST on the behavioral and psychological symptoms of dementia (BPSD) as a non-pharmacologic intervention will also be studied.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dementia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Community Site 5

CST Implementation community site

Group Type EXPERIMENTAL

Cognitive Stimulation Therapy

Intervention Type OTHER

Group-based therapy for people living with mild to moderate stage dementia, delivered by two trained facilitators.

Community Site 1

CST Implementation community site

Group Type EXPERIMENTAL

Cognitive Stimulation Therapy

Intervention Type OTHER

Group-based therapy for people living with mild to moderate stage dementia, delivered by two trained facilitators.

Community Site 2

CST Implementation community site

Group Type EXPERIMENTAL

Cognitive Stimulation Therapy

Intervention Type OTHER

Group-based therapy for people living with mild to moderate stage dementia, delivered by two trained facilitators.

Community Site 3

CST Implementation community site

Group Type EXPERIMENTAL

Cognitive Stimulation Therapy

Intervention Type OTHER

Group-based therapy for people living with mild to moderate stage dementia, delivered by two trained facilitators.

Community Site 4

CST Implementation community site

Group Type EXPERIMENTAL

Cognitive Stimulation Therapy

Intervention Type OTHER

Group-based therapy for people living with mild to moderate stage dementia, delivered by two trained facilitators.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Cognitive Stimulation Therapy

Group-based therapy for people living with mild to moderate stage dementia, delivered by two trained facilitators.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* established diagnosis of dementia or meets the criteria for dementia based on a positive screening test with clinical evidence of cognitive impairment affecting one or more ADL
* has a SLUMS score greater than 10.

Exclusion Criteria

* unable to hold a meaningful conversation,
* unable to hear well enough to participate in a small group discussion
* severe visual impairment that precludes ability to see most pictures
* unable to remain in a group setting for 45 minutes
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Duke University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Milta Little, DO

Role: PRINCIPAL_INVESTIGATOR

Duke University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Durham Center for Senior Life

Durham, North Carolina, United States

Site Status

Program for All Inclusive Care of the Elderly

Durham, North Carolina, United States

Site Status

The Forest at Duke

Durham, North Carolina, United States

Site Status

Program for All Inclusive Care of the Elderly

Greensboro, North Carolina, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Pro00106751

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Combined tDCS and Cognitive Training in Alzheimer's
NCT06861231 ENROLLING_BY_INVITATION NA
tDCS and CO-OP in Chronic Stroke
NCT04617548 COMPLETED PHASE1