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Alzheimer Patients and the Snoezelen Program

NCT00548951 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2015-12-16

No results posted yet for this study

Summary

To determine the connection between Social Withdrawal and Sensory Deprivation in elderly clients with Alzheimer's Type Dementia (i.e. how providing sensory stimulation might reduce social withdrawal).

Conditions

Interventions

OTHER

Snoezelen Room

Session in a Snoezelen room once per week for 12 weeks

OTHER

Snoezelen Room

Session in a Snoezelen room three times per week for 12 weeks

OTHER

Control

Receive no sessions in a Snoezelen Room.

Sponsors & Collaborators

  • Queen's University

    lead OTHER

Principal Investigators

  • Roumen V. Milev, MD · Queen's University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2005-09-30
Primary Completion
2006-12-31
Completion
2006-12-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00548951 on ClinicalTrials.gov