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The effectiveness of psychoeducation on caregivers of children with cerebral palsy

Investigation of the effect of psychoeducation program on anxiety, depression and Quality of life of caregivers of children with cerebral palsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181130041807N1
Enrollment
15
Registered
2019-02-07
Start date
2019-04-04
Completion date
Unknown
Last updated
2019-02-25

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

Conditions

Depression , Anxiety , Cerebral palsy. Cerebral palsy

Interventions

Intervention group: After providing initial information about the participants and obtaining informed consent, anxiety, depression and quality of life will be assessed by Beck Anxiety Inventory, Beck

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 40 Years

Inclusion criteria

Inclusion criteria: The age range of these carers will be between 25 and 40 years old. Children's age range will be 2-7 years old Children will be at the level of 3,4 or 5 of the Gross Motor Function Classification System (GMFCS) Carers have at least a fifth grade elementary degree. Detection of cerebral palsy is definite

Exclusion criteria

Exclusion criteria: Absence of a participant in a session of the sum of psychoeducational sessions Unwillingness to stay in research

Design outcomes

Primary

MeasureTime frame
Anxiety: A score that is obtained using the Beck Anxiety Scale. Timepoint: Before the intervention, immediately after the intervention and after a 2 month follow-up period. Method of measurement: Beck Anxiety questionnaire.;Depression: The score used by the Beck Depression questionnaire. Timepoint: Before the intervention, immediately after the intervention and after a 2 month follow-up period. Method of measurement: Beck Depression questionnaire.;Quality of Life: The score obtained using the SF36 questionnaire. Timepoint: Before the intervention, immediately after the intervention and after a 2 month follow-up period. Method of measurement: SF36 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlibakhshi Hossein

Semnan University of Medical Sciences

halibakhshi.m@gmail.com+98 23 3334 0867

Outcome results

None listed

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