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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02827474
Other study ID # UNMHSC- 16-111
Secondary ID
Status Completed
Phase N/A
First received July 1, 2016
Last updated February 14, 2018
Start date July 2016
Est. completion date January 20, 2018

Study information

Verified date February 2018
Source University of New Mexico
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Description:

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.

The investigators will conduct semi-structured interviews with patient participants and providers separately to determine patients' expectations of abortion care as well as the most important aspects of the abortion experience and to explore providers' perceptions of their patients' abortion experience and assess concordance.


Recruitment information / eligibility

Status Completed
Enrollment 34
Est. completion date January 20, 2018
Est. primary completion date January 20, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- 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.

Exclusion Criteria:

- 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.

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
United States Center for Reproductive Health Albuquerque New Mexico

Sponsors (1)

Lead Sponsor Collaborator
University of New Mexico

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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
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