COMPLETED

Enhancing Uptake of Preconception Care Services in Family Practice Clinics Using a Patient Centered Screening Tool

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

Sixteen years have passed since the Centers for Disease Control recommended routine preconception screening and counseling in primary care settings, yet time constraints and low preconception counseling adherence have prevented widespread uptake. This innovative, self-selected preconception screening tool encourages participants to be active in their own care and eliminates the time burden associated with typical pre-selected screening in clinics. This project will generate important knowledge about the promise of utilizing a participant-selected preconception screening tool to promote preconception health behavior change during routine medical encounters for women of reproductive age.

Official Title

Enhancing Uptake of Preconception Care Services in Family Practice Clinics Using a Patient Centered Screening Tool: A Pilot Study

Quick Facts

Study Start:2023-09-23
Study Completion:2025-08-26
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT06582160

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:19 Years to 49 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Biologically female
  2. * Child-bearing age
  3. * Visiting the clinic for a routine or preventative appointment during the study period
  1. * Under 19 or over 49 years of age
  2. * Not biologically female

Contacts and Locations

Principal Investigator

Shannon I Maloney, PhD
PRINCIPAL_INVESTIGATOR
University of Nebraska

Study Locations (Sites)

Nebraska Medicine - Fontenelle Clinic
Omaha, Nebraska, 68104
United States

Collaborators and Investigators

Sponsor: University of Nebraska

  • Shannon I Maloney, PhD, PRINCIPAL_INVESTIGATOR, University of Nebraska

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 Date2023-09-23
Study Completion Date2025-08-26

Study Record Updates

Study Start Date2023-09-23
Study Completion Date2025-08-26

Terms related to this study

Additional Relevant MeSH Terms

  • Women
  • Reproductive Age