Alzheimer Patients and the Snoezelen Program

This study has been completed.
Sponsor:
Information provided by:
Queen's University
ClinicalTrials.gov Identifier:
NCT00548951
First received: September 12, 2005
Last updated: August 19, 2008
Last verified: August 2008
  Purpose

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).


Condition Intervention Phase
Dementia
Other: Snoezelen Room
Other: Control
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: The Connection Between Sensory Deprivation and Social Withdrawal in Clients of a Long Term Care Facility Living With Alzheimer's Disease and the Effects of a Snoezelen Program.

Resource links provided by NLM:


Further study details as provided by Queen's University:

Primary Outcome Measures:
  • To evaluate improvement of the residents who are given Snoezelen sessions. [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Enrollment: 18
Study Start Date: September 2005
Study Completion Date: December 2006
Primary Completion Date: December 2006 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
Subject receives Snoezelen sessions once per week.
Other: Snoezelen Room
Session in a Snoezelen room once per week for 12 weeks
Active Comparator: 2
Subject receives Snoezelen sessions three times per week.
Other: Snoezelen Room
Session in a Snoezelen room three times per week for 12 weeks
3
Subject receives no sessions per week.
Other: Control
Receive no sessions in a Snoezelen Room.

Detailed Description:

The Snoezelen concept or program was originally thought up in Holland and comes from two Dutch words meaning to "sniff and doze". It was first introduced in the Netherlands in the 1970's. The first room was introduced in Snoezelen examines how a group of people react to an area that is private, relaxed and one that they trust. This program will bring out one's sense of taste, touch, smell, sight and hearing just by being in a specially designed room. Trust and relaxation will be looked at by those people with developmental disabilities (those that learn at a slower rate). Snoezelen originated with the belief that everyone needs nerve pulses (senses).

Inside a Snoezelen room you will find, dimmed lights, a relaxed atmosphere and pleasant surroundings, soothing sounds, intriguing aromas, tasty puddings, candies, interesting light effects (fiber optic light spray), comfortable seating, opportunities for interaction and engagement, sense of control over environment, tactile objects (awareness box), bubble tube, solar projector wheel, water fountain, massage pillow, massage tube, tranquility and solitude. The Snoezelen room is an environment in which the primary senses (see, hear, taste, touch) are stimulated all to create an environment that is both relaxing and stimulating. The benefits of Snoezelen change per person but may include some of the following:

  • Increased resident and caregiver communication
  • Increased awareness and understanding of the environment

The Snoezelen idea: client-controlled, safe comfortable atmosphere and freedom from pressure.

Sensory Deprivation (loss) The average person touches 300 different surfaces every 30 minutes. The average person with a profound disability will likely touch 1-5 surfaces in the same time frame.

  Eligibility

Ages Eligible for Study:   65 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Residents living at Rideaucrest Home (Long Term Care Facility in Kingston, Ontario);
  • Residents having a Mini Mental State Exam with a score of 15 to 27 reflecting mild to moderate dementia;
  • Male or female over 65 years of age;
  • Resident who are able to leave the terrace;
  • Resident who are not actively participating in Life Enrichment Programs;
  • Able to provide informed written and signed consent by resident or substitute decision maker.

Exclusion Criteria:

  • Suffering from severe life threatening illness with a reasonable expectation of death within the next six month;
  • Severe mental disorder in the opinion of the investigator (i.e. bipolar, schizophrenia);
  • No recent change in medication(s) during the past four weeks prior to the project;
  • Other non-Alzheimer-Type Dementia;
  • Residents who suffer from Epilepsy.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00548951

Locations
Canada, Ontario
Rideaucrest Home
Kingston, Ontario, Canada, K7K 3H6
Sponsors and Collaborators
Queen's University
Investigators
Principal Investigator: Roumen V. Milev, MD Queen's University
  More Information

No publications provided

Responsible Party: Dr. Roumen V. Milev, Queen's University
ClinicalTrials.gov Identifier: NCT00548951     History of Changes
Other Study ID Numbers: PSIY-205-05
Study First Received: September 12, 2005
Last Updated: August 19, 2008
Health Authority: Canada: Health Canada

Keywords provided by Queen's University:
Dementia

Additional relevant MeSH terms:
Dementia
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Delirium, Dementia, Amnestic, Cognitive Disorders
Mental Disorders

ClinicalTrials.gov processed this record on August 28, 2014