Social Interactions Between People With Dementia in Nursing Home

Sponsor
Paris West University Nanterre La Défense (Other)
Overall Status
Completed
CT.gov ID
NCT02403245
Collaborator
Radboud University Medical Center (Other)
60
2
35.1

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the direct impact of one session of social stimulation on social interactions of people with moderate dementia living in nursing home in comparison of one session without direct social stimulation.

Condition or Disease Intervention/Treatment Phase
  • Other: Psychosocial stimulation
N/A

Detailed Description

60 people with moderate dementia living in a french nursing homme participated in this study. Residents gave oral consent twice to participate. They were classified in groups of six residents taking into account socio-demographic and medical characteristics. Two experimental conditions were proposed : 1. a social stimulation session (36 residents) and 2. a control group without direct social stimulation (24 residents). Collected socio-demographic and medical characteristics are age, gender, timf of institutionalization, sociocultural level, marital status and diagnostic hypothesis. Before the study, scales and questionnaires were used to assess cognitive status with the Mini Mental State Examination (Folstein et al, 1975); functional abilities with Instrumental Activities of Daily Living (Lawton and Brody, 1969); depression with the Cornell Scale for Depression in Dementia (Alexopoulos et al, 1988); psychological and behavioural disorders with the Neuropsychiatric Inventory (Cummings et al, 1994); and the quality of life with the Alzheimer's Disease Related Quality of Life (Rabins et al, 1999).

Social interactions are video taped and analyzed in a grid of observation.

The aim of the study is to see if there is an impact on social interactions after just one social stimulation session compared to a control group situation. Expected results are that residents of the social stimulation group will have more social interactions between us than the resident of the control group.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Official Title:
The Impact of a Social Stimulation on Social Interactions in Institutionalized People With Dementia
Study Start Date :
Mar 1, 2012
Actual Primary Completion Date :
Jan 1, 2015
Actual Study Completion Date :
Feb 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Psychosocial stimulation

One session of a social stimulation

Other: Psychosocial stimulation
Intervention consists in a session of social stimulation during about 40 minutes through where the speaker introduced himself to the residents and introduces the residents to each others. The date of the day was done to residents. Social stimulation consists here to an exercise about the four seasons. Residents are asked to mention the 4 seasons and to give all the characteristics they can about each season. Two exercises were proposed: 4 pictures of landscapes and residents were asked to tell which season is represent on the pictures and pictures of some fruits and residents tried to tell in which season we find the fruits. Finally, the psychologist speaks about the "four season" of the compositor Vivaldi and propose to the residents to listen some extracts of each pieces of music.

No Intervention: Control group

Residents are in a social controlled condition but without direct stimulation.

Outcome Measures

Primary Outcome Measures

  1. Observed social behaviours [during 8 minutes before the session a]

    social behaviours of residents observed and listed in an observations grid to analyze the results from observation in terms of components of behaviours expressed in means of observed behaviours.

  2. Observed social behaviours [during 8 minutes after the session]

    social behaviours of residents observed and listed in an observations grid to analyze the results from observation in terms of components of behaviours expressed in means of observed behaviours.

Secondary Outcome Measures

  1. Cognitive Status [Baseline]

    Scale of the Mini Mental State of examination scored on 30 points.

  2. Functional abilities [Baseline]

    Scale of the Instrumental Activities of Daily Living scored on 14 points. More the score is high more the people is independent in daily living.

  3. Depression [Baseline]

    Cornell Scale for Depression in Dementia scored on 38 points. More the score os high more the people is depressed with a threshold score of 10.

  4. Psychological and behaviors disorders [Baseline]

    Neuropsychiatric Inventory : hetero-evaluation of the psychological and behavioural disorders in 12 domains with the frequency of occurrence of the disorder, the intensity and the resounding on caregivers.

  5. Quality of life [Baseline]

    Hetero-evaluation scale named Alzheimer's Disease Related Quality of life expressed in percentage. A high score means a good quality of life.

Eligibility Criteria

Criteria

Ages Eligible for Study:
75 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • presence of a diagnostic of dementia in medical report and a MMSE score between 9 and
Exclusion Criteria:
  • arrival in the institution dating less than six months

  • invalidating visual or hearing disorders

  • phasic disorders not allowing a minimum of communication

  • significant behavioural disorders (which can disturb the meeting)

  • residents not fluent in French language

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Paris West University Nanterre La Défense
  • Radboud University Medical Center

Investigators

  • Principal Investigator: Jean-Bernard Mabire, University Paris Ouest - EA 4430 - 200, Avenue de la République - 92001 Nanterre cedex

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jean-Bernard Mabire, psychologist and PhD psychologist Student, Paris West University Nanterre La Défense
ClinicalTrials.gov Identifier:
NCT02403245
Other Study ID Numbers:
  • SID010
First Posted:
Mar 31, 2015
Last Update Posted:
Mar 31, 2015
Last Verified:
Mar 1, 2015
Keywords provided by Jean-Bernard Mabire, psychologist and PhD psychologist Student, Paris West University Nanterre La Défense
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2015