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Efficacy of a psychoeducative intervention program to prevent or reduce the burden associated with caring for dementia patients

Efficacy of a psychoeducative intervention program to prevent or reduce the burden associated with caring for dementia patients: a two arm single blind, multicentre, randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14411440
Enrollment
238
Registered
2011-03-10
Start date
2009-09-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burden associated to dementia caregiving Nervous System Diseases

Interventions

Control group: Caregivers allocated to this group received the usual support from the day center or memory clinic where the patients had a multifaceted /multiprofessional care which aimed at reducing

Sponsors

Maria Josefa Recio Foundation - Institute of Psychiatric Research (Spain)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Males or females with age more than or equal to 18 years, giving care to a familiar person with a diagnosis of dementia according to Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM IV)-TR criteria 2. The caregiver was not profesionally paid for caregiving 3. The familiar diagnosed of dementia was receiving appropriate care as outpatient in a day center or memory clinic 4. The caregiver spend a minimum of 4 hours/day to care for the patient with dementia 5. The patient cared for had at least two instrumental activities impaired (a score of 0 in the Lawton & Brody scale) or one activity of daily life impaired (Katz index codes A or D) 6. Signed informed consent to participate in the trial

Exclusion criteria

Exclusion criteria: 1. Caregivers without time to attend the psychoeducative intervention training 2. Caregivers receiving currently or recently (last year), any standardised psychoeducative intervention similar to the one administered in the trial

Design outcomes

Primary

MeasureTime frame
Change since baseline to endpoint in the caregiver burden as assessed by the Zarit Burden Interview

Secondary

MeasureTime frame
1. Change since baseline to endpoint in the caregiver mental health as assessed by the General Health Questionnaire, 28 items 2. Change since baseline to endpoint in the caregiver quality of life as assessed by the SF-12

Countries

Portugal, Spain

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 10, 2026