A program to help caregivers of children with cancer manage anxiety and build resilience
Brief Intervention to Reduce Anxiety and Promote Resilience in Caregivers of Youth With Cancer
This study is testing a new online program to help caregivers of children with cancer manage their anxiety and build resilience during a tough time.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 8 Years to 18 Years |
| Sex | All |
| Sponsor | Stanford University Academic / other |
| Locations | 1 site (San Francisco, California) |
| Trial ID | NCT05415007 on ClinicalTrials.gov |
What this trial studies
This study examines a brief psychotherapeutic and psycho-educational intervention designed for caregivers of youth recently diagnosed with cancer. The intervention is delivered in a virtual setting and aims to assess its feasibility and accessibility as a preliminary step toward a larger efficacy trial. The study focuses on understanding the impact of the intervention on caregiver psychological distress, including anxiety, depression, and post-traumatic stress disorder, while also exploring family stress and the need for mental health services in pediatric oncology.
Who should consider this trial
Good fit: Ideal candidates for this study are caregivers of children aged 0-17 who have received a cancer diagnosis within the past 12 months and are fluent in English.
Not a fit: Patients who may not benefit from this study include those who are not caregivers of children with cancer or those who do not meet the inclusion criteria.
Why it matters
Potential benefit: If successful, this program could significantly improve the mental health and quality of life for caregivers of children with cancer.
How similar studies have performed: Other studies have shown success with similar psycho-educational interventions for caregivers, indicating potential for positive outcomes in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion and Exclusion Criteria: Parents Inclusion * Child (0-17yrs) with recent (\<12 mo) cancer diagnosis * Fluent in English * Consent to research Exclusion: * Lack of proficiency in written and spoken English * Parent is under age 18 * Active Suicidal Ideation * Child with cancer does not provide assent Inclusion and Exclusion Criteria: Children Inclusion: * Recent (\<12 mo) cancer diagnosis in child * 8-17 Years old * Provides assent to participate in the study Exclusion: * Cannot read English * Parent is not enrolled in the study Anyone who is not a caregiver of children who have been diagnosed with cancer within the past 12 months will be excluded.
Where this trial is running
San Francisco, California
- Stanford Cancer Institute — San Francisco, California, United States (Recruiting)
Study contacts
- Principal investigator: Victoria E. Cosgrove, PhD — Stanford University
- Study coordinator: Victoria E. Cosgrove, PhD
- Email: veileen@stanford.edu
- Phone: 650-995-6848
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.