An observational study in Pregnancy Termination, sponsored by University of New Mexico. Completed at 1 site in United States. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2018-02-15.
Sponsored by University of New Mexico · Observational
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 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.
University of New Mexico is the lead sponsor of 306 studies on the registry; 28 are open to participants now.
Of its 25 completed or terminated interventional studies of FDA-regulated products, 23 (92%) have results posted.
Counted across the registry records on this site, refreshed daily.
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.
Exclusion Criteria:
Patient participants will participate in two patient interviews.
Other: Patient Interview
Provider participants will participate in one provider interview.
Other: Provider 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.
For physician participants, providers will be interviewed after completion of the patient's visit and this will be 10-15 minutes.
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.
Time frame: One year
Plan to share: No
No publications or documents are linked to this record.
This study is completed, as verified in Feb 2018. You cannot join it, but the record below documents what was studied.
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University of New Mexico