RECRUITING

Family Foundations for Individuals Pregnant Via ART

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

The purpose of this study is to help expectant mothers build a coparenting bond and improve communication with a support person (co-caregiver). Participation will include completing two online surveys (one at 12-30 weeks gestation \& one at 3 months postpartum), providing two at-home bloodspot collections and returning the collections via mail. Studies suggest that stress increases inflammation. Investigators aim to explore this by collecting a small amount of blood at the first and last session. Participants will also attend 9 virtual one-two hour Family Foundations (FF) intervention sessions (at no cost to participants) with a supportive co-caregiver. Total time commitment will be 18 hours, max, over a 6 month period.

Official Title

Family Foundations for Individuals Pregnant Via Assisted Reproductive Technology

Quick Facts

Study Start:2025-06-11
Study Completion:2028-01-30
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06770972

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:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Pregnant individuals via ART, at least 18 years of age
  2. 2. Have a caregiving partner (e.g. spouse, grandparent; nanny; friend) who will attend sessions
  3. 3. Provision of signed and dated informed consent form
  4. 4. Stated willingness to comply with all study procedures and availability for the duration of the study
  5. 5. English speaking
  1. 1. Psychosis
  2. 2. Perinatal loss (current) - history of loss is OK
  3. 3. Individuals outside of the US
  4. 4. Do not have smartphones, tablets, computers (the FF class is virtual)

Contacts and Locations

Study Contact

Pearl Heumann, BS
CONTACT
323-866-8107
familyfoundations@cshs.org

Study Locations (Sites)

Cedars Sinai Medical Center
Los Angeles, California, 90048
United States

Collaborators and Investigators

Sponsor: Cedars-Sinai Medical 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 Date2025-06-11
Study Completion Date2028-01-30

Study Record Updates

Study Start Date2025-06-11
Study Completion Date2028-01-30

Terms related to this study

Keywords Provided by Researchers

  • Assisted Reproductive Technology
  • mental health outcomes
  • pregnancy

Additional Relevant MeSH Terms

  • Assisted Reproductive Technology