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Efficacy of psychosocial intervention for psychological burden in families of schizophrenic patients

Efficacy of psycho- social intervention for psychological burden in families of schizophrenic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203129267N1
Enrollment
40
Registered
2014-05-16
Start date
2013-03-09
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

Schizophrenia. Schizophrenia, schizotypal and delusional disorders

Interventions

Intervention 1: Intervention group will be assigned in 4 subgroups of 5 individuals, then will attend in 3 stages of psychosocial intervention. First stage contains 1 section in introducing the proces
Rehabilitation
Intervention group will be assigned in 4 subgroups of 5 individuals, then will attend in 3 stages of psychosocial intervention. First stage contains 1 section in introducing the process. The second st

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1- definite diagnosis of schizophrenia or schizo-affective disorders through a psychiatrist; 2- a family member who lives with patient and/or be responsible for caring the patient; 3- a family member who would like to attain and participate in psychosocial intervention and assign the consent form. Exclusion criteria: 1- learning disability diagnosed through a psychiatrist; 2- personality disorders diagnosed through a psychiatrist that could interfere with psychosocial intervention.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Family burden. Timepoint: immedietly, 1month, 6 months, 1 year after finishing the intervention. Method of measurement: Family Burden Questionnaire.

Secondary

MeasureTime frame
Recurrence of the disorder. Timepoint: immediately, 1 month, 6 months, 1 year after finishing the intervention. Method of measurement: examining the times of hospitalization.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGiti Setoodeh

Shiraz University of Medical Sciences

setoodeh@sums.ac.ir+98 71 1647 4256

Outcome results

None listed

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