COMPLETED

Protective Assets Reinforced With Integrated Care and TechnologY (PARITY) Feasibility Trial

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 determine the feasibility and acceptability of the Protective Assets Reinforced with Integrated care and TechnologY (PARITY) program, to test the clinical, behavioral, and strength building efficacy of the PARITY program and explore how it achieves its outcomes in pregnant Black women. PARITY is a program that provides community-based doula support, community resources, and a mobile technology platform that reinforces individual strengths (referred to as protective assets) through positive messaging and by promoting wellness.

Official Title

Protective Assets Reinforced With Integrated Care and TechnologY (PARITY) Feasibility Trial

Quick Facts

Study Start:2023-04-06
Study Completion:2025-08-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05802615

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 51 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Black race
  2. * Pregnant with gestational age 20-28 weeks at enrollment
  3. * Ability to read and write in English language
  4. * Planning to give birth at a healthcare facility \& receive obstetrical care with a healthcare record
  5. * Reside within 20 minutes of the Lincoln/Omaha, NE metro area
  6. * Owns a smartphone with internet access
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Principal Investigator

Elizabeth K Mollard, PhD
PRINCIPAL_INVESTIGATOR
University of Nebraska

Study Locations (Sites)

University of Nebraska Medical Center
Omaha, Nebraska, 68198
United States

Collaborators and Investigators

Sponsor: University of Nebraska

  • Elizabeth K Mollard, 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 Date2023-04-06
Study Completion Date2025-08-06

Study Record Updates

Study Start Date2023-04-06
Study Completion Date2025-08-06

Terms related to this study

Additional Relevant MeSH Terms

  • Maternal Health
  • Blood Pressure