- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04803045
Does a Brief Intervention Decrease Patient Drop Out Rates?
18. marts 2021 opdateret af: Boston IVF
The Impact of a Brief Intervention on Retention Rates With Patients Who Did Not Return to Care After an Initial Physician Visit
The goal of this study is to determine a) if a follow-up email to selected patients who had an initial consult with an infertility specialist, but did not return for a second visit, would change return to care behavior and b) why patients had not returned.
Studieoversigt
Detaljeret beskrivelse
From July 2017 to March 2018 all patients who had attended an initial visit with an infertility specialist at the clinic, but had not returned for at least three months were selected to receive a follow up email.
Those selected for an email excluded patients who the Investigator's knew had achieved a pregnancy, already had a plan for treatment, had visited for an egg freeze and all LGTBQ patients.
The email asked if the patient had any questions about that visit, offered support to the patient and included contact information for the patient liaison sending the email.
The email also asked each participant to indicate why they had not returned and were provided 4 options and an opportunity to write in a response.
From April 2018 to December 2018 no emails were sent to patients.
No other change of patient contact practice was initiated during the trial period.
This study will observe routine to care behavior of these patients after 11 months post initial consult date.
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
647
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
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Massachusetts
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Waltham, Massachusetts, Forenede Stater, 02451
- Boston IVF
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Kvinde
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Female patients attending an initial consult at Boston IVF between set dates.
Beskrivelse
Inclusion Criteria:
- Female patients attending an initial consult with a physician at Boston IVF and were recommended to continue care with the clinic
Exclusion Criteria:
- Patients who the Investigators knew had achieved a pregnancy
- Patients who already had a plan for treatment in place after their initial consult
- Patients who had visited for an egg freeze
- LGTBQ patients
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
---|---|
Follow Up Email
Patients received a follow up email 3 months after an initial consult with a physician but did not return to care.
|
Patients received an email 3 months after an initial consult asking why they had not returned to care.
Patients were provided with 4 options and a space to write in comments.
The email asked if the patient had any questions and offered support.
|
No follow up
Patients who did not receive any follow up after their initial consult, following clinic standard of care.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Return to care behavior
Tidsramme: 11 months after initial consult
|
The study will track if the patient return to care rate
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11 months after initial consult
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Alice Domar, PhD, Boston IVF
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. juli 2017
Primær færdiggørelse (Faktiske)
1. januar 2019
Studieafslutning (Faktiske)
1. marts 2020
Datoer for studieregistrering
Først indsendt
15. marts 2021
Først indsendt, der opfyldte QC-kriterier
15. marts 2021
Først opslået (Faktiske)
17. marts 2021
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
22. marts 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
18. marts 2021
Sidst verificeret
1. marts 2021
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- DomarRTC
Plan for individuelle deltagerdata (IPD)
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