COMPLETED

MA-ASAP at Independent Abortion Clinics: A Demonstration Project

Conditions

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

In this study, the investigators propose to conduct a parallel study to MA-ASAP (ClinicalTrials.gov Identifier: NCT05278780) at an independent clinic.

Official Title

Medication Abortion With Autonomous Self-Assessment Project at Independent Abortion Clinics: A Demonstration Project

Quick Facts

Study Start:2023-02-16
Study Completion:2023-06-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05781061

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:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Can speak and read English
  2. * Has an address in a state where the study clinicians are licensed to practice medicine and where the service is legal
  3. * Is old enough to consent to abortion and study participation without parental consent in the study state
  4. * Has reviewed the study website
  5. * Has had a positive pregnancy test
  6. * Has signed the study informed consent form (ICF), which will be included within the questionnaire
  7. * Is pregnant with a gestational age of ≤77 days from last menstrual period
  8. * Desires MA
  9. * Has no symptoms of or risk factors for ectopic pregnancy
  10. * Has no medical contraindications to MA, specifically:
  11. * Is not asked by the site to have a synchronous consultation with clinician OR facility-based tests such as ultrasound, laboratory tests, examination, etc.
  12. * Is comfortable obtaining the abortion pills without a pre-treatment ultrasound and without speaking by phone or video with the abortion provider.
  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

Study Locations (Sites)

All Families Healthcare
Whitefish, Montana, 59937
United States

Collaborators and Investigators

Sponsor: Gynuity Health Projects

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 Date2023-02-16
Study Completion Date2023-06-15

Study Record Updates

Study Start Date2023-02-16
Study Completion Date2023-06-15

Terms related to this study

Additional Relevant MeSH Terms

  • Abortion Early