ACTIVE_NOT_RECRUITING

Roadmap to Parenthood: Testing the Efficacy of a Decision Aid and Planning Tool for Family Building After Cancer

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Conditions

Quality of LifeParenthood StatusRoadmap to ParenthoodDecision aidPlanning tool

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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 study will test a decision support intervention that consists of a web-based 'decision aid and planning tool' for family building after cancer in a randomized controlled trial.

Official Title

Roadmap to Parenthood: Testing the Efficacy of a Decision Aid and Planning Tool for Family Building After Cancer

Quick Facts

Study Start:2024-05-20
Study Completion:2026-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06050135

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 to 45 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Assigned female at birth
  2. * Aged 18 to 45 years old
  3. * Understands verbal and written English
  4. * History of a cancer diagnosis.
  5. * Completed cancer treatment(s) with known or uncertain gonadotoxic effects (e.g., systemic chemotherapy, surgery or radiation affecting reproductive organs or hormone regulation, stem cell or bone marrow transplant, and/or immunotherapy)
  6. * Interested in having a future child (or more children) or uncertain about family building plans
  7. * Access to the Internet and use of a computer, tablet, or smartphone
  8. * Ability to understand and the willingness to personally sign the written IRB-approved informed consent document
  1. * Currently undergoing cancer treatment excluding long term adjuvant or maintenance therapies, such as tamoxifen
  2. * Significant physical or mental disability that prevents completion of study activities

Contacts and Locations

Principal Investigator

Catherine Benedict, PhD
PRINCIPAL_INVESTIGATOR
Stanford University

Study Locations (Sites)

Stanford Universtiy
Palo Alto, California, 94305
United States

Collaborators and Investigators

Sponsor: Stanford University

  • Catherine Benedict, PhD, PRINCIPAL_INVESTIGATOR, Stanford University

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 Date2024-05-20
Study Completion Date2026-12

Study Record Updates

Study Start Date2024-05-20
Study Completion Date2026-12

Terms related to this study

Keywords Provided by Researchers

  • Roadmap to Parenthood
  • Decision aid
  • Planning tool

Additional Relevant MeSH Terms

  • Quality of Life
  • Parenthood Status