RECRUITING

Parenting Support Intervention for Families Coping With Metastatic or Locally Recurrent Solid Tumor Diagnosis

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Parenting Support Intervention for Families Coping With an Advanced Cancer Diagnosis

Quick Facts

Study Start:2021-11-30
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05059678

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients must be diagnosed with a metastatic or locally recurrent solid malignant tumor
  2. * Patients must be at least 18 years old
  3. * Patients must have at least one dependent child between the ages of 4 and 12 and currently living with the parent
  4. * Patients must be able to provide informed consent
  5. * 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
  6. * Patients with cognitive deficits that would impede the completion of self-report instruments as measured by the Mini Mental State Examination (score of =\< 17)
  1. * Patients and caregivers who do not read and speak English and who do not have access to the internet

Contacts and Locations

Study Contact

Kathrin Milbury
CONTACT
713-745-2868
kmilbury@mdanderson.org

Principal Investigator

Kathrin Milbury
PRINCIPAL_INVESTIGATOR
M.D. Anderson Cancer Center

Study Locations (Sites)

M D Anderson Cancer Center
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: M.D. Anderson Cancer Center

  • Kathrin Milbury, PRINCIPAL_INVESTIGATOR, M.D. Anderson Cancer Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-11-30
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2021-11-30
Study Completion Date2026-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Metastatic Malignant Solid Neoplasm
  • Recurrent Malignant Solid Neoplasm