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Focus: Pre-residency Intention to Provide AbortionNCT01763073

Beliefs and Practice Intentions of Future Ob/Gyn Residents Regarding Reproductive Healthcare

An observational study of Focus: Pre-residency Intention to Provide Abortion, run by Brigham and Women's Hospital at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective of this study is to ascertain factors shaping medical students' pre-residency intention to provide abortion through an in-depth qualitative investigation into the context and experiences that shape intention to provide. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
How many people
74 participants
Where
1 siteUnited States
Study dates
Jan 2013to Feb 2022
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Fourth-year students in accredited US medical schools who have applied to, but not yet been matched with, residency programs in obstetrics and gynecology.

Who may be able to join

  • current 4th-year medical student
  • US accredited medical school
  • has applied to, but not yet been accepted into, obstetrics and gynecology residency programs

Who cannot join

  • age less than 18 years
  • former student reapplying to residency (e.g., not current 4th-year student)
  • has not yet applied to residency
  • has already been accepted to residency

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Brigham and Women's Hospital

    Boston, Massachusetts, 02120

Other trials in United States

About this study

The objective of this study is to ascertain factors shaping medical students' pre-residency intention to provide abortion through an in-depth qualitative investigation into the context and experiences that shape intention to provide.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01763073
Study groupRoleWhat they receive
Medical StudentsFourth-year students in accredited US medical schools who have applied to, but not yet been matched with, residency programs in obstetrics and gynecology.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Factors affecting pre-residency intention to provide abortion

    Factors will be identified by systematically coding qualitative data using a combination of deductive and inductive analytical strategies.

    Measured: Up to 15 months. Each participant will be interviewed once, between January and March 2013 or between September 2013 through March 2014.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted8 Jan 2013 (estimated)
  2. Study startJan 2013
  3. Primary completionFeb 2022
  4. Study completionFeb 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
74 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01763073
Sponsor's protocol ID
2012P001794
Status last verified
Feb 2023
First submitted
3 Jan 2013
Last updated
8 Feb 2023
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Focus: Pre-residency Intention to Provide Abortion, run by Brigham and Women's Hospital at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Feb 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Factors affecting pre-residency intention to provide abortion (time frame: Up to 15 months. Each participant will be interviewed once, between January and March 2013 or between September 2013 through March 2014.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Feb 2023; AzTrials last refreshed its copy on 8 Nov 2026.

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