Metastatic Malignant Solid Neoplasm Clinical Trial
Official title:
Parenting Support Intervention for Families Coping With an Advanced Cancer Diagnosis
This clinical trial examines the acceptability and effect of a parenting support intervention for families coping with solid tumor that has spread to other places in the body (metastatic) or has come back (recurrent). Parenting support program may help to reduce common parenting concerns, improve communication between parents and children about cancer, and improve the overall psychological wellbeing of parents.
| Status | Recruiting |
| Enrollment | 120 |
| Est. completion date | December 31, 2026 |
| Est. primary completion date | December 31, 2026 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - Patients must be diagnosed with a metastatic or locally recurrent solid malignant tumor - Patients must be at least 18 years old - Patients must have at least one dependent child between the ages of 4 and 12 and currently living with the parent - Patients must be able to provide informed consent - Patients must have a spousal caregiver over the age of 18 who co-parents the child(ren) (i.e. share custody) and is willing and able to consent to participate - Patients with cognitive deficits that would impede the completion of self-report instruments as measured by the Mini Mental State Examination (score of =< 17) Exclusion Criteria: - Patients and caregivers who do not read and speak English and who do not have access to the internet |
| Country | Name | City | State |
|---|---|---|---|
| United States | M D Anderson Cancer Center | Houston | Texas |
| Lead Sponsor | Collaborator |
|---|---|
| M.D. Anderson Cancer Center | National Cancer Institute (NCI) |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Examine the feasibility of implementing a parenting support intervention in 50 patients with an incurable cancer and their spousal caregivers. | Through study completion, an average of 1 year |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
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