- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03774368
Targeted Video Messaging About Emergency Contraception
15 juli 2019 uppdaterad av: Planned Parenthood League of Massachusetts
Targeted Video Messaging About Emergency Contraception Via a Social Media Platform
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).
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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).
The investigators will assess whether a video or website link has superior reach, engagement, and return on investment (measured as cost per click) through a Facebook ad campaign.
The investigators will also ensure that both modalities of consumer engagement (website and video) are efficacious at ensuring adequate and improved knowledge of emergency contraception through a laboratory-environment trial.
Studietyp
Interventionell
Inskrivning (Faktisk)
150
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
-
-
Massachusetts
-
Boston, Massachusetts, Förenta staterna, 02215
- PPLM
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 29 år (Vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Kvinna
Beskrivning
Inclusion Criteria:
- Women
- 18 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
Exclusion Criteria:
- 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
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Övrig
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
---|---|
Övrig: Website about emergency contraception
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.
|
Existing website with factual information about emergency contraception
|
Övrig: Video about emergency contraception
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.
|
Existing video with factual information about emergency contraception
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Emergency contraception knowledge (binary)
Tidsram: Immediately after intervention
|
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
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Copper IUD as emergency contraception knowledge
Tidsram: Immediately after intervention
|
This outcome is a binary outcomes that reflects a participant's ability to correctly identify the copper IUD as emergency contraception, when to use it, and how to access it.
|
Immediately after intervention
|
Levonorgestrel pill as emergency contraception knowledge
Tidsram: Immediately after intervention
|
This outcome is a binary outcomes that reflects a participant's ability to correctly identify the levonorgestrel pill as emergency contraception, when to use it, and how to access it.
|
Immediately after intervention
|
Ulipristal pill as emergency contraception knowledge
Tidsram: Immediately after intervention
|
This outcome is a binary outcomes that reflects a participant's ability to correctly identify the ulipristal pill as emergency contraception, when to use it, and how to access it.
|
Immediately after intervention
|
Emergency contraception knowledge (continuous)
Tidsram: Immediately after intervention
|
This outcome reflects the participant's overall knowledge of emergency contraception after the website or video intervention, as measured by the proportion of questions they get correct on the survey
|
Immediately after intervention
|
Change in emergency contraception knowledge pre- and post-intervention
Tidsram: Immediately before and immediately after intervention
|
This outcome reflects the participant's change in knowledge of emergency contraception before and after the website or video intervention, as measured by the proportion of questions they get correct on the survey.
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Immediately before and immediately after intervention
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Likelihood of using emergency contraception pre- and post-intervention
Tidsram: Immediately before and immediately after intervention
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This outcome reflects the participant's likelihood of using emergency contraception both before and after the intervention, as measured on a 6 point likert scale (I would definitely use it, Very likely, Somewhat likely, Somewhat unlikely, Very unlikely, I definitely would NOT use it)
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Immediately before and immediately after intervention
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Utredare
- Huvudutredare: Principal Investigator, MD, Planned Parenthood League of Massachusetts
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
15 januari 2019
Primärt slutförande (Faktisk)
7 juni 2019
Avslutad studie (Faktisk)
7 juni 2019
Studieregistreringsdatum
Först inskickad
11 december 2018
Först inskickad som uppfyllde QC-kriterierna
11 december 2018
Första postat (Faktisk)
13 december 2018
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
16 juli 2019
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
15 juli 2019
Senast verifierad
1 juli 2019
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 2018P001764
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .
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