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Clinical traial of the effect of education on Alzheimer's caregiver's burden

Effect of cognitive-behavioral management education on Alzheimer's family caregiver's burden

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014081818847N1
Enrollment
70
Registered
2015-01-09
Start date
2014-09-10
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Alzheimer's. Alzheimer disease, unspecified

Interventions

Behavior
Intervention 1: Intervention group: At first caregiver's burden will be measured by the questionnaire then the cognitive-behavioral management training will be provided for this group. This education
Intervention group: At first caregiver's burden will be measured by the questionnaire then the cognitive-behavioral management training will be provided for this group. This education will be in 4 ses
Control group: In control group, there will be no interventions. The burden questionnaire will be answered by the participants in this group and 6 weeks after training finished in intervention group,

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: Having informed consent; Being relatives of the patient; Being the main caregiver; Caring of the patient at least for 6 months and a maximum period of 1 year; Having the capacity to respond to the questionnaire; The patient should be in second stage of Alzheimer's disease (stage of cognitive behavioral disorders); The caregiver not being affected by any mental illnesses and do not use any drugs. Exclusion criteria: Death of the patient with Alzheimer; The participant not interested in continuing the practice; Entrust the care of patient with Alzheimer to other health facilities or other people.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Burden. Timepoint: Before the intervention and 6 weeks after the intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLadan Bagherbeik Tabrizi

Tehran University of Medical Sciences

Ladanbagherbeik@gmail.com; Ladanbagherbeik@yahoo.com+90 218 877 05 99

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026