Evaluation of a Decision Aid for Early Pregnancy Loss
Primary Purpose
Early Pregnancy Loss
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Healthwise Decision Aid
Control informational handout
Sponsored by
About this trial
This is an interventional health services research trial for Early Pregnancy Loss
Eligibility Criteria
Inclusion Criteria:
- English speaking
- Definitive diagnosis of early intrauterine pregnancy loss (including anembryonic pregnancy and missed abortion [ultrasound examination demonstrates fetal pole without cardiac activity measuring between 5.3 and 7mm or an abnormal growth pattern diagnostic of EPL])
- 18 years or older
- Willing and able to give informed consent
Exclusion Criteria:
- Pregnancy of unknown anatomic location
- Unable to read English
- Prior options counseling with a Family Planning provider
- Clinically unstable requiring emergent surgical management with uterine evacuation.
Sites / Locations
- Hospital of the University of Pennsylvania
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Intervention
Control
Arm Description
Standard counseling + Healthwise Decision Aid
Standard counseling + a control informational handout.
Outcomes
Primary Outcome Measures
Decision Conflict Scale (DCS)
Low-literacy version of Decision Conflict Scale
Secondary Outcome Measures
Full Information
NCT ID
NCT04410029
First Posted
May 18, 2020
Last Updated
March 26, 2021
Sponsor
University of Pennsylvania
Collaborators
Society of Family Planning
1. Study Identification
Unique Protocol Identification Number
NCT04410029
Brief Title
Evaluation of a Decision Aid for Early Pregnancy Loss
Official Title
Evaluation of a Decision Aid for Early Pregnancy Loss: a Pilot RCT Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
July 29, 2020 (Actual)
Primary Completion Date
March 23, 2021 (Actual)
Study Completion Date
March 25, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Pennsylvania
Collaborators
Society of Family Planning
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims to determine the effect of the Healthwise decision aid on shared decision making in women undergoing management of early pregnancy loss.
Detailed Description
Early pregnancy loss (EPL) or miscarriage is a common problem occurring in 15-20% of pregnancies. EPL can safely be managed surgically, medically, or expectantly; patient preferences, together with provider recommendations, should be used to guide treatment decisions. The three management options differ substantially experientially for patients. Previous literature has shown that patients have preferences for treatment and higher satisfaction when treated according to their preferences. Decision aids provide individualized information to help patients clarify their priorities and personal values. There is good evidence that decision aids compared to usual care resulted in greater knowledge, more realistic expectations, lower decisional conflict relating to feeling informed, more active decision making, less people remaining undecided, and greater effect agreement on value and choice. Despite this, there is limited research on the extent of decisional conflict experienced by women undergoing treatment for EPL, or the effect of decision aids on decisional conflict. Furthermore, only a few decision aid tools are publicly available for this indication. The Healthwise decision aid tool receives high scores by the International Patient Decision Aid Standards Scale, and is readily available to patients within the clinical site's electronic medical record.
The investigators propose a pilot randomized control trial, enrolling 50 participants with EPL. The study will measure baseline decisional conflict, and randomize participants to counseling with or without the decision aid. The investigators intend to study the Decisional Conflict Scale at baseline and after counseling, knowledge scores, Decision Regret and the 9-item Shared Decision Making Questionnaire (SDM-Q9) after counseling. Study data can be used to inform future research and to identify patients with predictors for high decisional conflict. This study is the first step towards validation of a high-quality decision aid tool for patients undergoing EPL management. It will also be the first study to report on decisional conflict and regret in patients with early pregnancy loss.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Early Pregnancy Loss
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Standard counseling + Healthwise Decision Aid
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Standard counseling + a control informational handout.
Intervention Type
Other
Intervention Name(s)
Healthwise Decision Aid
Intervention Description
Healthwise, a non-profit company that develops health content and patient information for hospitals, has created a decision aid for EPL management that is available through the EPIC Systems, an electronic medical record. Participants will be given this decision aid after EPL diagnosis and prior to options consultation with a provider.
Intervention Type
Other
Intervention Name(s)
Control informational handout
Intervention Description
Participants randomized to the control arm will be given an informational handout of treatment options after EPL diagnosis and prior to options consultation with a provider.
Primary Outcome Measure Information:
Title
Decision Conflict Scale (DCS)
Description
Low-literacy version of Decision Conflict Scale
Time Frame
Post-counseling (one day)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
English speaking
Definitive diagnosis of early intrauterine pregnancy loss (including anembryonic pregnancy and missed abortion [ultrasound examination demonstrates fetal pole without cardiac activity measuring between 5.3 and 7mm or an abnormal growth pattern diagnostic of EPL])
18 years or older
Willing and able to give informed consent
Exclusion Criteria:
Pregnancy of unknown anatomic location
Unable to read English
Prior options counseling with a Family Planning provider
Clinically unstable requiring emergent surgical management with uterine evacuation.
Facility Information:
Facility Name
Hospital of the University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19143
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Evaluation of a Decision Aid for Early Pregnancy Loss
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