NCT03774368

Brief Summary

This research study will assess the real-world effectiveness of Facebook advertising as a strategy to reach women of reproductive age who are at risk of unintended pregnancy with a brief educational intervention about emergency contraception (EC).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2019

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 11, 2018

Completed
2 days until next milestone

First Posted

Study publicly available on registry

December 13, 2018

Completed
1 month until next milestone

Study Start

First participant enrolled

January 15, 2019

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 7, 2019

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 7, 2019

Completed
Last Updated

July 16, 2019

Status Verified

July 1, 2019

Enrollment Period

5 months

First QC Date

December 11, 2018

Last Update Submit

July 15, 2019

Conditions

Outcome Measures

Primary Outcomes (1)

  • Emergency contraception knowledge (binary)

    This outcome is a binary outcome that reflects a participant's ability to correctly identify an emergency contraceptive method, when to use it, and how to access it

    Immediately after intervention

Secondary Outcomes (6)

  • Copper IUD as emergency contraception knowledge

    Immediately after intervention

  • Levonorgestrel pill as emergency contraception knowledge

    Immediately after intervention

  • Ulipristal pill as emergency contraception knowledge

    Immediately after intervention

  • Emergency contraception knowledge (continuous)

    Immediately after intervention

  • Change in emergency contraception knowledge pre- and post-intervention

    Immediately before and immediately after intervention

  • +1 more secondary outcomes

Study Arms (2)

Website about emergency contraception

OTHER

Subjects are randomly assigned to view an existing website about emergency contraception. The website contains information about the three methods of emergency contraception: the copper IUD, ulipristal pill, and levonorgestrel pill. It includes information about their relative effectiveness and where to access emergency contraception.

Other: Emergency contraception website

Video about emergency contraception

OTHER

Subjects are randomly assigned to view an existing video about emergency contraception. The video is two minutes in length and contains information about the three methods of emergency contraception: the copper IUD, ulipristal pill, and levonorgestrel pill. It includes information about their relative effectiveness and where to access emergency contraception.

Other: Emergency contraception video

Interventions

Existing website with factual information about emergency contraception

Website about emergency contraception

Existing video with factual information about emergency contraception

Video about emergency contraception

Eligibility Criteria

Age18 Years - 29 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Women
  • to 29 years old
  • Living or seeking care in or around Boston, MA
  • Able to participate in an in-person visit at Planned Parenthood League of Massachusetts (PPLM) Boston Health Center
  • English fluency
  • Have at least one social media account (i.e. Facebook, Instagram, Twitter, Pinterest, YouTube, Snapchat)
  • Endorse using social media at least once a week

You may not qualify if:

  • PPLM staff
  • Currently or ever employed in the reproductive health field
  • Currently using long-acting reversible contraception (LARC)
  • History of permanent sterilization (by participant or sexual partner)
  • Previous participation in the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

PPLM

Boston, Massachusetts, 02215, United States

Location

Study Officials

  • Principal Investigator, MD

    Planned Parenthood League of Massachusetts

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 11, 2018

First Posted

December 13, 2018

Study Start

January 15, 2019

Primary Completion

June 7, 2019

Study Completion

June 7, 2019

Last Updated

July 16, 2019

Record last verified: 2019-07

Data Sharing

IPD Sharing
Will not share

Locations