Experimental Study of the Impact of a Group Therapy Psychological Intervention for Caregivers of Alzheimer's Disease Patients

Not Applicable

Completed

• Conditions: Psychological Support to Caregivers of Azlheimer's Patients
• Interventions: Behavioral: Cognitive Behavioral Therapy Group

• Registration Number: NCT01762618
• Lead Sponsor: Barcelonabeta Brain Research Center, Pasqual Maragall Foundation

Brief Summary

A randomized controlled trial designed to test the effectiveness of a psychological intervention based on group therapy for the caregivers of Alzheimer's disease patients. The intervention consists of 14 sessions of a cognitive-behavioral psychological group therapy. This study aims to demonstrate that Alzheimer's patients' caregivers can benefit from group counseling, with an improvement in mood state, quality of life, perceived burden and a decrease in anxiety and depression. Two evaluations will be done: before the therapy sessions (basal) and when intervention is finished (final).

Detailed Description

The aim of this study is to conduct group therapy with Alzheimer's caregivers at three centers in the province of Barcelona: Hospital El Carme Badalona, Sanitary Center of Les Corts and Sarrià.

The therapy sessions are conducted by an expert in group therapy (from the sponsor Pasqual Maragall Foundation) and the social worker of each of the centers. The study takes place for four months and consists of weekly therapy sessions of an hour and a half each (14 sessions in total), based on cognitive and behavioral theory. The participants and the control group are evaluated at the beginning and at the end of the study in terms of mood, quality of life, anxiety and depression.

This study aims to demonstrate that Alzheimer's patient's caregivers can benefit from group counseling, resulting in an improvement in their emotional state, perceived burden, quality of life and a more positive attitude coping with the new situation.

Study Timeline

• Study Start: 2012-01
• Study First Submitted: 2012-12-18
• Study First Submitted QC: 2013-01-04
• Study First Posted: 2013-01-08
• Primary Completion: 2013-04
• Study Completion: 2013-07
• Status Verified: 2014-07
• Last Update Submitted: 2014-07-08
• Last Update Posted: 2014-07-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 83

Inclusion Criteria

• To be the principal caregiver of a person with Alzheimer's disease
• The patient has a possible or probable diagnosis of Alzheimer's disease made for an Accredited Dementia Unit.
• The patient score in the Global Deterioration Scale must be: 4, 5 or 6A.
• The caregiver must dedicate at least 5 hours a day or spend a significant part of his time to care-related tasks
• The caregiver must sign the Informed Consent

Exclusion Criteria

• To receive a financial compensation for the care of the patient
• The caregiver or the patient has a psychiatric illness according to the DSM-IV TR, such that the investigator considers it might hinder the dynamics of the group and affect the objectives of the study
• Be receiving some type of formal counseling (conducted by a therapist

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Cognitive Behavioral Therapy Group	Cognitive Behavioral Therapy Group	14 therapy sessions, once a week for one and a half hours.

Primary Outcome Measures

Name	Time	Method
Change from baseline in POMS Scale ("Profile of Mood States")	Pre-treatment and 4 weeks post treatment	Change from baseline compared to the control and active arms using the Profile of Mood State (POMS) validated in structure and content for the Spanish language. This scale is a popular instrument for mood evaluation. It comprises 44 items (with a Likert response from 0 to 4), representing six conceptual dimensions: tension, depression,anger, vigour, fatigue and friendliness.

Secondary Outcome Measures

Name	Time	Method
Change from baseline compared to the control and active arms using the Martin and cols. scale to assess the overload level of the family caregivers of patients with probable or possible Alzheimer's disease or other advanced stage dementia.	Pre-treatment and 4 weeks post treatment	Martin and cols. scale is an adaptation of the Zarit questionnaire to assess the overload level of the caregiver. It is a self administered questionnaire, with 22 items with each item scored from 1 ('none') to 5 ('nearly always').

Trial Locations

Locations (3)

Primary Assistant Center Les Corts; 🇪🇸 Barcelona, Catalonia, Spain

Hospital del Carme; 🇪🇸 Badalona, Barcelona, Spain

Primary Assistant Center Sarrià; 🇪🇸 Barcelona, Catalonia, Spain