Skip to main content
Clinical Trials/NCT01689948
NCT01689948
Terminated
Not Applicable

Alzheimer Disease : Rehabilitation's Intervention at Home. A Preliminary Pilot Study.

Nantes University Hospital1 site in 1 country17 target enrollmentOctober 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alzheimer's Disease
Sponsor
Nantes University Hospital
Enrollment
17
Locations
1
Primary Endpoint
Evaluation of the mean scores of Instrumental Activities of Daily Living (IADL)
Status
Terminated
Last Updated
11 years ago

Overview

Brief Summary

Alzheimer's disease (AD) is the most common cause of dementia among elderly patients. By its prevalence and its medical and social consequences, AD represents a dual challenge to public health and society. The elderly want to stay in their homes even when their lives are altered by a chronic progressive disease. Their caregivers claim in turn a support at home. But this desire is questioned because of the characteristics of the disease, e.g. the altered relational function by the cognitive impairment and the behavioural disorders associated.

Outpatients non-drug therapies represent a potential support that adapts to patient with an AD or mixed dementia, especially in their milder forms.

The aim of the study is to evaluate the feasibility of a weekly rehabilitation's intervention at home and its acceptability by both the patient and the caregiver.

The study of its efficiency in terms of autonomy will be the next step.

Detailed Description

The protocol is based on weekly rehabilitation's intervention at home. All home visits and assessments of the patient and his caregiver will be made by the rehabilitation's therapist himself. Twelve weekly interventions at home are planed. The first five are needed to define a realistic and achievable goal of treatment which is accepted by the dyad and the therapist. The following seven interventions will achieve this goal by rehabilitation's intervention (e.g. occupational therapy, psychomotor approach). Four filmed sessions for dyad's assessment are planned (at inclusion, at weeks 5 and 12 after inclusion and 3 months after the last intervention).

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
September 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Evaluation of the mean scores of Instrumental Activities of Daily Living (IADL)

Time Frame: 27 weeks

The main objective is to compare the mean scores of Instrumental Activities of Daily Living (IADL) observed at inclusion (day 0) with those observed 27 weeks later (meaning 3 months after the last of the twelfth weekly session of at home rehabilitation therapy).

Secondary Outcomes

  • Evaluation of the mean scores of Instrumental Activities of Daily Living (IADL)(13 weeks)
  • Evaluation of the mean scores of Neuro Psychiatric Inventory (NPI)(13 weeks)
  • Evaluation of the mean scores of Zarit's scale (caregiver burden)(5 weeks)
  • Alcohol consumption for the patient and the caregiver(27 weeks)
  • Evaluation of the mean scores of Mini Mental State Examination (MMSE)(meaning evaluation of patient's cognitive impairment)(27 weeks)
  • Evaluation of the mean scores of Goal Attainment scales (GAS) (meaning evaluation of the satisfaction of the patient and of her/his caregiver)(27 weeks)

Study Sites (1)

Loading locations...

Similar Trials