ClinicalTrials.Veeva

Menu

Web-based Psycho-Educational Program to Support Carers of Alzheimer's Patients (DIAPASON)

A

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Alzheimer Disease

Treatments

Behavioral: Consultation in memory clinic
Behavioral: psycho-social intervention based on a web-based psycho-educational program, called Diapason.

Study type

Interventional

Funder types

Other

Identifiers

NCT01430286
P081002

Details and patient eligibility

About

The aim of the project is to evaluate the efficacy of a web-based psycho-educational programme designed to support informal caregivers of patients with Alzheimer's disease (AD).This program focuses on information about the illness, her progression, how to prevent psychological strain using anticipation and relaxation techniques and providing a virtual space (forum) to discuss with other caregivers.

Full description

Context: Since some of the ICs do not have the possibility to participate in face-to-face interventions, information and communication technologies are being increasingly used for a distance intervention. Research showing the benefit of a combined approach including psycho-social interventions for caregivers and Information and Communication Technologies (ICT) in the caring of Alzheimer's disease patients is actually growing. Main objective: To evaluate the efficacy of a a web-based psycho-educational program designed to support carers of AD patientsMethodology: This is a randomized clinical trial . 80 participants will be randomized in 2 parallel groups: The volunteers in the experimental condition (EC) should visit at least one time per week the website of program, during 12 weeks. Each week a new thematic is added to the website. b) The participants in the control group (CG) will receive a minimal intervention, and will have access to the Diapason program after their participation (six months). Caregivers are recruited (according to exclusion and inclusion criteria) and followed up in memory center participating in the trial.

Evaluation criteria:

Primary criteria:

  • Perceived Stress Scale (PSS-14).

Secondary evaluation criteria:

  • Nottingham Health Profile (NPH),
  • Zarit Burden Interview (BI),
  • Revised Memory and Behavior Problems Checklist (RMBPC),
  • Beck Depression Inventory (BDI-2) Mediator variables
  • Revised Scale for Caregiving Self-Efficacy (RCSE).
  • Statistics of website utilization Controlled variables
  • Sociodemographic variables (Self report)
  • Knowledge about illness (Visual analogical scale - VAS)
  • The quality of the relationship with the patient (VAS)
  • Time spent on caregiving
  • Other sources of stress (i.e. work, health status, financial status)
  • Respite or social help (i.e. psychotherapy, associations, technical help, etc)
  • Cognitive and autonomy status of patient (MMSE and IADL)

Statistical analysis by the department of biostatistics and medical computing of the Hospital Cochin will be performed.

Enrollment

49 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria :

  • Family caregivers of AD patients DSM IV-TR (American Psychiatric Association 2004) or NINCDS/ADRDA (McKhann et al. 1984).
  • Age: over 18 years old
  • score 12 or over on the Perceived Stress Scale 14 items (PSS-14, Cohen) Need for information or help
  • Sign informed consent

Exclusion criteria :

  • Professional or paid caregiver
  • Physical or mental disease incompatible with patient's management
  • Impossibility to participate in the educational program
  • Absence of perceived stress
  • Ongoing psychotherapy or a similar program in parallel

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

49 participants in 2 patient groups

Psycho-educational program
Experimental group
Description:
This group is trained for a 3 month period by a web-based psycho-educational program, Lifestyle Counseling, etc.
Treatment:
Behavioral: psycho-social intervention based on a web-based psycho-educational program, called Diapason.
Standard treatment
Active Comparator group
Description:
This group will receive treatment as usual : consultation in memory clinic every 6 months during the AD patient's consultation.
Treatment:
Behavioral: Consultation in memory clinic

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems