- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02827474
We Experience: Perspectives on a Quality Abortion Care Experience: A Patient Centered Approach
Perspectives on a Quality Abortion Care Experience: A Patient Centered Approach
Study Overview
Status
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
New Mexico
-
Albuquerque, New Mexico, United States, 87106
- Center for Reproductive Health
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
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.
Description
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 Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patient Participants
Patient participants will participate in two patient interviews.
|
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.
|
Physician Participants
Provider participants will participate in one provider interview.
|
For physician participants, providers will be interviewed after completion of the patient's visit and this will be 10-15 minutes.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient Experience, semi-structured interviews
Time Frame: One year
|
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
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Brenda Pereda, MD, University on New Mexico
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- UNMHSC- 16-111
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Pregnancy Termination
-
Centre Hospitalier Universitaire DijonRecruitingMedical Termination of Pregnancy | Voluntary Termination of PregnancyFrance
-
Gynuity Health ProjectsCompletedPregnancy TerminationVietnam, Tunisia
-
Hospices Civils de LyonCompletedMedical Termination of PregnancyFrance
-
University of New MexicoSociety of Family PlanningWithdrawnPregnancy TerminationUnited States
-
Kanuni Sultan Suleyman Training and Research HospitalUnknown
-
Gynuity Health ProjectsCompletedTermination of PregnancyUnited States
-
Gynuity Health ProjectsCompletedTermination of PregnancyUnited States, Moldova, Republic of, Nepal
-
University Hospital, MontpellierCompletedTermination of PregnancyFrance
Clinical Trials on Patient Interview
-
The Christie NHS Foundation TrustCellCentric Ltd.Not yet recruitingMultiple MyelomaUnited Kingdom
-
Hospices Civils de LyonCompletedRheumatic Diseases | Treatment AdherenceFrance
-
Hospices Civils de LyonCompleted
-
Centre Hospitalier Intercommunal CreteilRecruitingBariatric SurgeryFrance
-
Oslo University HospitalRecruitingPostoperative Pain | Postoperative NauseaNorway
-
Tata Memorial HospitalCompleted
-
Harvard Pilgrim Health CareDepression and Bipolar Support Alliance; NAMI: National Alliance on Mental...CompletedBipolar Disorder
-
Kantonsspital Winterthur KSWCompleted
-
University of ChicagoCompleted
-
University Hospital, ToulouseCompletedIndolent Systemic Mastocytosis | Cutaneous MastocytosisFrance