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Medication Safety and Contraceptive Counseling for Reproductive Aged Women With Psychiatric Conditions

NCT02292056 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2014-11-17

No results posted yet for this study

Summary

There is currently limited research that addresses the unique medication safety and family planning needs among women of reproductive age with psychiatric conditions. The study will research the feasibility of a novel individualized 1-on-1 counseling session at the Gifford Clinic in the Department of Psychiatry at UCSD that will help women in this population better understand: 1) which of their medications are safe to use in pregnancy, 2) provide education regarding the importance of using contraception and which contraceptive choices are available to them, and 3) raise awareness of any drug-drug interactions that may exist between their medications and their chosen method of contraception. Patients will be given questionnaire to assess their contraceptive utilization. They will also be given a before and after quiz to allow for an objective measure of the patient's increase in knowledge regarding medication safety and contraceptive choices as a result of the investigators intervention.

Conditions

  • Mental Disorders
  • Contraception
  • Chemical Teratogen Exposure

Interventions

BEHAVIORAL

1-on-1 counseling

1. Precounseling questionnaire collecting demographic information, contraception information, and reasons for choosing contraceptive method 2. Precounseling quiz: assess baseline level of knowledge regarding medication safety and contraceptive option. 3. Counseling: completed by MotherToBaby counselor about the safety of their medications for use in pregnancy. 4. 10 minute video entitled "The Contraceptive Choice Project: Which Birth Control Method is Right for You?" by Washington University in St. Louis. 5. Post-Counseling Quiz to assess whether specialized training impacted their understanding of medication safety and contraceptive options. 6. Post-Counseling Questionnaire: assess contraceptive plans and satisfaction with counseling

Sponsors & Collaborators

Principal Investigators

  • Sheila Mody, MD MPH · UCSD Department of Reproductive Medicine

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2015-10-31
Completion
2015-10-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02292056 on ClinicalTrials.gov