Ignite Creation Date:
2024-05-06 @ 6:47 PM
Last Modification Date:
2024-10-26 @ 2:54 PM
Study NCT ID:
NCT05783310
Status:
COMPLETED
Last Update Posted:
2024-02-20
First Post:
2023-03-02
Brief Title:
Psychoeducation Intervention for Caregivers of Children With Cancer
Sponsor:
Chinese University of Hong Kong
Organization:
Chinese University of Hong Kong
Study Overview
Official Title:
Effectiveness of Psychoeducation Intervention on Reducing Negative Psychological Outcomes and Enhancing Coping of Caregivers of Children With Cancer A Randomized Controlled Trial
Status:
COMPLETED
Status Verified Date:
2024-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This randomized controlled trial aims to evaluate the effectiveness of the psychoeducation intervention on anxiety depressive symptoms coping and HRQoL in caregivers of children with cancer
The study is a two-arm parallel-group single-blind randomized controlled trial that will be conducted in two hospitals in Malawi
The study is a two-arm parallel-group single-blind randomized controlled trial that will be conducted in two hospitals in Malawi
Detailed Description:
Aim of the study To develop and implement psychoeducation intervention that meet the need of caregivers of children with cancer in Malawi
Objectives of the study
1 To develop a psychoeducation intervention that addresses the needs of caregivers of children with cancer in Malawian culture
2 To evaluate the effectiveness of the PEI in reducing anxiety and depressive symptoms and enhancing coping and HRQoL among caregivers of children with cancer in Malawi
Hypotheses of the study
1 Compared with the control group caregivers in the intervention group will have significantly lower anxiety levels immediately after the intervention and at 3 months post-intervention
2 Compared with the control group caregivers in the intervention group will have significantly fewer depressive symptoms immediately after the intervention and at 3 months post-intervention
3 Compared with the control group caregivers in the intervention group will have significantly better HRQoL immediately after the intervention and at 3 months post-intervention
4 Compared with the control group caregivers in the intervention group will have significantly better coping skills immediately after the intervention and at 3 months post-intervention
Objectives of the study
1 To develop a psychoeducation intervention that addresses the needs of caregivers of children with cancer in Malawian culture
2 To evaluate the effectiveness of the PEI in reducing anxiety and depressive symptoms and enhancing coping and HRQoL among caregivers of children with cancer in Malawi
Hypotheses of the study
1 Compared with the control group caregivers in the intervention group will have significantly lower anxiety levels immediately after the intervention and at 3 months post-intervention
2 Compared with the control group caregivers in the intervention group will have significantly fewer depressive symptoms immediately after the intervention and at 3 months post-intervention
3 Compared with the control group caregivers in the intervention group will have significantly better HRQoL immediately after the intervention and at 3 months post-intervention
4 Compared with the control group caregivers in the intervention group will have significantly better coping skills immediately after the intervention and at 3 months post-intervention
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None