The Influence of Trust in the Health Care System on Postpartum Contraceptive Choice

Sponsor
Medical University of South Carolina (Other)
Overall Status
Completed
CT.gov ID
NCT02213874
Collaborator
Society of Family Planning (Other)
208
1
1
36
5.8

Study Details

Study Description

Brief Summary

The purpose of this research is to understand the relationship between trust in the health care system and choice of contraception during the postpartum period among pregnant women receiving prenatal care.

Research subjects will complete a questionnaire at enrollment and between delivery and within 5 days of hospital discharge.

A chart review will also be completed to gather use of a birth control method at the six week postpartum visit as well as pertinent medical diagnoses and recorded data such as height, weight, body mass index, and contraceptive plan as documented in the postpartum medical chart.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaire
N/A

Detailed Description

The aims of the proposed research are three-fold:
  1. To identify whether trust in the health care system is associated with choice of the highest efficacy contraception (intrauterine contraception, implantable contraception, and sterilization) in the immediate postpartum period among pregnant women receiving prenatal care.

  2. To explore which patient-level factors (sociodemographic, reproductive history, future pregnancy intentions) and provider-level factors (antenatal contraceptive counseling) are associated with choice of the highest efficacy contraception in the immediate postpartum period among pregnant women receiving prenatal care.

  3. To determine whether trust in the health care system is altered during the receipt of prenatal care or delivery.

Study Design

Study Type:
Interventional
Actual Enrollment :
208 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
The Influence of Trust in the Health Care System on Postpartum Contraceptive Choice
Study Start Date :
Jan 1, 2012
Actual Primary Completion Date :
Jan 1, 2015
Actual Study Completion Date :
Jan 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Other: Questionnaire

A questionnaire will be administered during the early stages of prenatal care & again during the postpartum period. The initial questionnaire will assess trust in the health care system, locus of control, religiosity, health literacy & collect information about demographics, contraceptive & reproductive history, future pregnancy intentions, & baseline knowledge about contraception. The postpartum questionnaire will repeat questions about future pregnancy & contraception intentions, trust in the health care system, knowledge of contraception and collect new information about characteristics of antenatal contraceptive counseling received including whether a provider recommended a specific method of contraception, the amount of counseling received, & the type of counseling received.

Other: Questionnaire
A questionnaire will be administered during the early stages of prenatal care & again during the postpartum period. The initial questionnaire will assess trust in the health care system, locus of control, religiosity, health literacy & collect information about demographics, contraceptive & reproductive history, future pregnancy intentions, & baseline knowledge about contraception. The postpartum questionnaire will repeat questions about future pregnancy & contraception intentions, trust in the health care system, knowledge of contraception and collect new information about characteristics of antenatal contraceptive counseling received including whether a provider recommended a specific method of contraception, the amount of counseling received, & the type of counseling received.

Outcome Measures

Primary Outcome Measures

  1. Choice of long acting contraception (IUD or implant) for postpartum contraception [immediately postpartum]

    Using a questionnaire adminstered immediately postpartum, we will ascertain whether participants indicate plan to use either an IUD or implant for contraception. We will also measure use of IUD or implant through chart abstraction of their 6 week postpartum visit.

Secondary Outcome Measures

  1. Trust in the health care system [immediately postpartum]

    We will also evaluate trust as an outcome and evaluate whether certain patient-level or antepartum care characteristics predict higher levels of trust. Trust is measured through a validated scale containing 17 questions measured using a likert scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Pregnant Women receiving prenatal care at Medical University of South Carolina (MUSC)

  • Age 18 or older

Exclusion Criteria:
  • Greater than 20 weeks gestation

Contacts and Locations

Locations

Site City State Country Postal Code
1 MUSC Women's Health Charleston South Carolina United States 29425

Sponsors and Collaborators

  • Medical University of South Carolina
  • Society of Family Planning

Investigators

  • Principal Investigator: Angela Angela Dempsey, MD, Medical University of South Carolina

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dempsey, Associate Professor, Medical University of South Carolina
ClinicalTrials.gov Identifier:
NCT02213874
Other Study ID Numbers:
  • Dempsey-Trust Pro 12660
First Posted:
Aug 12, 2014
Last Update Posted:
May 11, 2018
Last Verified:
May 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Dempsey, Associate Professor, Medical University of South Carolina

Study Results

No Results Posted as of May 11, 2018