NCT02827474

Brief Summary

The purpose of this study is to determine aspects of abortion care most important to the patient in creating a "high quality" abortion experience, to investigate patients' expectations of abortion care, and to explore provider perceptions of patients' abortion experiences and assess concordance with patients' perspectives.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
34

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jul 2016

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

July 1, 2016

Completed
Same day until next milestone

Study Start

First participant enrolled

July 1, 2016

Completed
10 days until next milestone

First Posted

Study publicly available on registry

July 11, 2016

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 20, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 20, 2018

Completed
Last Updated

February 15, 2018

Status Verified

February 1, 2018

Enrollment Period

1.6 years

First QC Date

July 1, 2016

Last Update Submit

February 14, 2018

Conditions

Outcome Measures

Primary Outcomes (1)

  • Patient Experience, semi-structured interviews

    The investigators will use semi-structured interviews to determine aspects of abortion care most important to the patients in creating a "high quality" abortion experience.

    One year

Study Arms (2)

Patient Participants

Patient participants will participate in two patient interviews.

Other: Patient Interview

Physician Participants

Provider participants will participate in one provider interview.

Other: Provider Interview

Interventions

Patient intervention includes a 30 minute interview prior to their abortion procedure and a follow up phone-interview that will be 10-minutes and held 24-72 hours from the procedure.

Patient Participants

For physician participants, providers will be interviewed after completion of the patient's visit and this will be 10-15 minutes.

Physician Participants

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

Patient Participants: Women presenting to Center for Reproductive Health (CRH) for induced abortion for an undesired pregnancy in the first trimester \< 14 weeks and age 18-45 years. Woman must have a completed surgical abortion procedure and be able to speak English or Spanish. Provider Participants: Providers must be performing procedures on the day patient participants are recruited and must be willing to give their perspective on the participating patients' abortion experience.

You may qualify if:

  • Women presenting to the Center for Reproductive Health (CRH) for induced abortion for an undesired pregnancy in the first trimester \< 14 weeks.
  • Women ages 18-45 years.
  • Woman must have a completed surgical abortion procedure
  • Women must be able to speak English or Spanish.

You may not qualify if:

  • Women who are unable or unwilling to consent for the study or are unable or unwilling to complete a follow-up interview
  • Women who are unable to consent and/or are cognitively impaired.
  • Women who are under the age of 18
  • Women who are incarcerated.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Center for Reproductive Health

Albuquerque, New Mexico, 87106, United States

Location

Study Officials

  • Brenda Pereda, MD

    University on New Mexico

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 1, 2016

First Posted

July 11, 2016

Study Start

July 1, 2016

Primary Completion

January 20, 2018

Study Completion

January 20, 2018

Last Updated

February 15, 2018

Record last verified: 2018-02

Data Sharing

IPD Sharing
Will not share

Locations