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The effect of group psychoeducational program on caregiverburden and quality of life for families of children & adolescents with epilepsy

The effect of group psychoeducational program on caregiverburden and quality of life for families of children & adolescents with epilepsy admitted to selected centers of Isfahan University of Medical Sciences in 2017 – 2018

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017080335483N1
Enrollment
70
Registered
2017-09-15
Start date
2017-09-23
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

Epilepsy. Epilepsy

Interventions

Intervention 1: The researcher of his intervention program, which is a supportive educational tool, performs in 8 ( 90-minute ) sessions for family members of children and adolescents with epilepsy wh
The researcher of his intervention program, which is a supportive educational tool, performs in 8 ( 90-minute ) sessions for family members of children and adolescents with epilepsy who are eligible

Sponsors

Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Entry criterion: Family care is considered as the main caregiving agent of the patient and they have a great deal of responsibility. In each family, the one who is the main caregiver, attends the study; he or she must not be drug-addicted and not to be treated with psychosocial drugs. The must not have participated in family education meetings. (any other researcher project in this field); there must be only one chronic caregiver in the family; must not have psychosocial problems that may cause the disease to develop; they must have at least one year of patient care; patients must be aged 6-18 years, the caregiver age is over 18 and under 65 years old. Exclusion criteria: there are physical and psychological problems that cannot continue to participate in the study; they have irregular participation in the sessions (having more than two absences).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Caregiver burden. Timepoint: Before, immediately after and one months after the intervention. Method of measurement: zarit burden Questionnaire.

Secondary

MeasureTime frame
Quality of life. Timepoint: Before, immediately after and one month after the intervention. Method of measurement: WHOQOL-BREF instrument.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSaied Pahlavanzadeh

Isfahan University of Medical Sciences

pahlavanzadeh@nm.mui.ac.ir+98 31 3668 7124

Outcome results

None listed

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