A Resilience Promotion Program for Parents of Children With Cancer

Parents of Children With Cancer Clinical Trial

Official title:

A Resilience Promotion Program for Parents of Children With Cancer

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04038242
• Other study ID #: UW 19-436
• Status: Completed
• Phase: N/A
• Start date: August 13, 2019
• Est. completion date: July 21, 2020

Study information

• Verified date: October 2020
• Source: The University of Hong Kong
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cancer is a leading cause of death for children. With the increasing incidence of childhood cancer, the mental health problems emerge in those parents struggle with their children's life-threatened disease. Caring for children with cancer is described as life-changing experience and overwhelming stress for parents. Many studies have been conducted to screen the psychological distress for these parents and found a considerable percentage of them suffering from depressive symptoms. Poorer quality of life was also found in parents of children with cancer when compared to parents of children without cancer. Additionally, parental distress interacted with children's emotions and could have detrimental effects on children's both physical and mental health. Therefore, it is important to take measures improving the mental health for parents of children with cancer.

Although current various psychological interventions illustrated small to moderate improvements of mental health for parents of children with cancer, the total effect base on a systematic review was not statistically significant. The purpose of these interventions was predominantly to treat negative mental health problems such as depression and no recognized effective psychological interventions were available for parents of children with cancer until now. Along with the paradigm shift from problem-oriented approach to nurturing strengths in the post-modern period, instead of exclusively treating mental health problems, researchers payed more attention to positive therapy such as resilience promotion program. Resilience usually refers to the ability to adapt adverse conditions and maintain positive status. Resilience studies are mounting since the flourishing of positive psychology movement and meaningful results were gained from corresponding intervention program concentrating on resilience promotion in adolescent education, handling chronic disease and recovery of breast cancer. However, there is a lack of targeted resilience promotion program for parents of children with cancer. The results of our pilot study showed low levels of resilience in parents of children with cancer and strong associations among parental resilience, quality of life and depression. It indicates that the increase in resilience can benefit for the mental health of parents. Therefore, a resilience promotion program will be conducted to examine efficacy for parents of children with cancer.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 103
• Est. completion date: July 21, 2020
• Est. primary completion date: July 21, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• having a child (0-19 years old) with cancer diagnosis.

• Chinese resident and able to read Chinese and speak Mandarin.

Exclusion Criteria:

• having physical impairment or cognitive and learning problems identified from family history of medical records.

• attending other researches.

Related Conditions & MeSH terms

• Parents of Children With Cancer

Intervention

Other:
• Resilience promotion program
Resilience Promotion Program consists of eight sessions. Except the first orientation session and the last review session, other six sessions focus on cultivating the five internal resiliency factors (physical, behavioral, cognitive, emotional and spiritual). There are two sessions for behavioral factor, including one special to deal with the relationships between parents and children.

Locations

Country	Name	City	State
Hong Kong	University of Hong Kong	Hong Kong

Sponsors (1)

Lead Sponsor	Collaborator
The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in levels of resilience from baseline to 6-month follow-up between intervention and control group	The primary outcome measure is the resilience of subjects at 6-month follow-up when compare to baseline. The Connor-Davison resilience scale will be used to assess participants' resilience. The total score ranges from 0-100 and higher score reflecting higher levels of resilience.	6-month follow-up
Secondary	Levels of resilience at baseline	The Connor-Davison resilience scale will be used to assess participants' resilience. The total score ranges from 0-100 and higher score reflecting higher levels of resilience.	baseline
Secondary	Change in levels of resilience from baseline to 2-month follow-up between intervention and control group	The Connor-Davison resilience scale will be used to assess participants' resilience. The total score ranges from 0-100 and higher score reflecting higher levels of resilience.	2-month follow-up
Secondary	Levels of quality of life at baseline	The Short Form of Medical Outcomes will be used to measure quality of life. The total score ranges from 0.32 for the worst health state to 1 for full health.	baseline
Secondary	Change in levels of quality of life from baseline to 2-month follow-up between intervention and control group	The Short Form of Medical Outcomes will be used to measure quality of life. The total score ranges from 0.32 for the worst health state to 1 for full health.	2-month follow-up
Secondary	Change in levels of quality of life from baseline to 6-month follow-up between intervention and control group	The Short Form of Medical Outcomes will be used to measure quality of life. The total score ranges from 0.32 for the worst health state to 1 for full health.	6-month follow-up
Secondary	Levels of depression at baseline	Self-rating depression scale will be used to measure depression. The total score ranges from 20 to 80. Higher total score indicates more serious depression status.	baseline
Secondary	Change in levels of depression from baseline to 2-month follow-up between intervention and control group	Self-rating depression scale will be used to measure depression. The total score ranges from 20 to 80. Higher total score indicates more serious depression status.	2-month follow-up
Secondary	Change in levels of depression from baseline to 6-month follow-up between intervention and control group	Self-rating depression scale will be used to measure depression. The total score ranges from 20 to 80. Higher total score indicates more serious depression status.	6-month follow-up
Secondary	Levels of anxiety at baseline	Self-rating anxiety scale will be used to measure anxiety. The total score ranges from 25 to 100 and higher score reflects worse anxiety status.	baseline
Secondary	Change in levels of anxiety from baseline to 2-month follow-up between intervention and control group	Self-rating anxiety scale will be used to measure anxiety. The total score ranges from 25 to 100 and higher score reflects worse anxiety status.	2-month follow-up
Secondary	Change in levels of anxiety from baseline to 6-month follow-up between intervention and control group	Self-rating anxiety scale will be used to measure anxiety. The total score ranges from 25 to 100 and higher score reflects worse anxiety status.	6-month follow-up
Secondary	Levels of stress at baseline	The perceived stress scale will be used to measure stress. The total score ranges from 0 to 40. Higher total score suggests more perceived stress.	baseline
Secondary	Change in levels of stress from baseline to 2-month follow-up between intervention and control group	The perceived stress scale will be used to measure stress. The total score ranges from 0 to 40. Higher total score suggests more perceived stress.	2-month follow-up
Secondary	Change in levels of stress from baseline to 6-month follow-up between intervention and control group	The perceived stress scale will be used to measure stress. The total score ranges from 0 to 40. Higher total score suggests more perceived stress.	6-month follow-up