- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01433185
Improving Uptake of Early Infant Diagnosis of HIV for the Prevention of Mother-to-child Transmission of HIV (SMS4PMTCT)
19. januar 2015 opdateret af: Thomas Odeny, University of Washington
Improving Uptake of Early Infant Diagnosis of HIV for PMTCT: a Randomized Trial of a Text Messaging Intervention
Early accurate diagnosis is one of the first crucial steps in care for infants born to HIV-infected mothers.
Early initiation of antiretroviral therapy (ART) relies upon early diagnosis and results in significant reductions in infant morbidity and mortality.
There is little information on evidence-based interventions that specifically target improved attendance of postpartum clinic visits and subsequent infant HIV testing in the context of prevention of mother-to-child transmission of HIV (PMTCT) programs.
The investigators propose a randomized controlled trial to examine the effect of text messages sent to women enrolled in PMTCT programs on adherence to postpartum clinic visits and uptake of early infant diagnosis by DNA polymerase chain reaction (PCR).
This study seeks to test the hypotheses that (a) text messages sent to women enrolled in PMTCT will improve their attendance at the postnatal clinic within the first 6-8 weeks after childbirth; and (b) text messages sent to women enrolled in PMTCT programs will increase uptake of DNA PCR HIV testing at 6-8 weeks among infants exposed to HIV.
This study will evaluate a novel strategy to improve adherence to postnatal clinic visits and increase the uptake of infant HIV testing.
If proven superior to standard care, the proposed intervention can be easily scaled-up and integrated into existing healthcare systems in resource-limited settings.
Findings from this study will provide randomized trial evidence to inform HIV prevention program planners and implementers.
This study will also provide further information on the feasibility of using mobile phone-based technology for public health interventions in resource-limited settings.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
388
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Nyanza
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Kisumu, Nyanza, Kenya
- Kenya Medical Research Institute, Family AIDS Care and Education Services
-
-
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
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Kvinde
Beskrivelse
Inclusion Criteria:
- age at least 18 years
- report ability to read SMS
- ≥ 28 weeks gestation or delivery at study clinic on day of enrollment
- HIV positive women enrolled in the PMTCT program
- have access to a mobile phone (personal or partner's if HIV serostatus disclosed to partner)
- willing to receive SMS messages from the study
- planning to remain in the study area (Nyanza province) for the duration of the study
Exclusion Criteria:
- age less than 18 years old
- women who share phones with partners but HIV status not disclosed to partners
- intention to deliver at a non-study hospital
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Text message (SMS)
Text messages sent to women before and after delivery
|
Text messages sent to women before and after delivery
Andre navne:
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|
Ingen indgriben: Usual care (current standard of care)
Current standard of care for women enrolled in PMTCT programs
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Proportion of women who attend postnatal clinic within 6-8 weeks postpartum
Tidsramme: 6-8 weeks after delivery
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6-8 weeks after delivery
|
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Proportion of infants tested for HIV by DNA PCR
Tidsramme: 6-8 weeks after delivery
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6-8 weeks after delivery
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Infant adherence to antiretroviral prophylaxis
Tidsramme: Up to 6 weeks after delivery
|
Up to 6 weeks after delivery
|
|
Time to post-natal clinic return
Tidsramme: Up to 8 weeks after delivery
|
Up to 8 weeks after delivery
|
|
Maternal adherence to antiretroviral prophylaxis
Tidsramme: Up to 8 weeks after delivery
|
Up to 8 weeks after delivery
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studiestol: Elizabeth A Bukusi, MBChB, MMed, MPH, PhD, Kenya Medical Research Institute
- Ledende efterforsker: Thomas A Odeny, MBChB, MPH, University of Washington/Kenya Medical Research Institute
- Studiestol: R Scott McClelland, MD, MPH, University of Washington
- Studiestol: Craig R Cohen, MD, MPH, University of California, San Francisco
- Studiestol: Carol Camlin, PhD, University of California, San Francisco
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Odeny TA, Bukusi EA, Cohen CR, Yuhas K, Camlin CS, McClelland RS. Texting improves testing: a randomized trial of two-way SMS to increase postpartum prevention of mother-to-child transmission retention and infant HIV testing. AIDS. 2014 Sep 24;28(15):2307-12. doi: 10.1097/QAD.0000000000000409.
- Odeny TA, Newman M, Bukusi EA, McClelland RS, Cohen CR, Camlin CS. Developing content for a mHealth intervention to promote postpartum retention in prevention of mother-to-child HIV transmission programs and early infant diagnosis of HIV: a qualitative study. PLoS One. 2014 Sep 2;9(9):e106383. doi: 10.1371/journal.pone.0106383. eCollection 2014.
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
1. april 2012
Primær færdiggørelse (Faktiske)
1. juli 2013
Studieafslutning (Faktiske)
1. juli 2013
Datoer for studieregistrering
Først indsendt
12. september 2011
Først indsendt, der opfyldte QC-kriterier
12. september 2011
Først opslået (Skøn)
13. september 2011
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
21. januar 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. januar 2015
Sidst verificeret
1. januar 2015
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- RNA-virusinfektioner
- Virussygdomme
- Infektioner
- Blodbårne infektioner
- Overførbare sygdomme
- Seksuelt overførte sygdomme, virale
- Seksuelt overførte sygdomme
- Lentivirus infektioner
- Retroviridae infektioner
- Sygdomme i immunsystemet
- Langsomme virussygdomme
- HIV-infektioner
- Erhvervet immundefektsyndrom
- Immunologiske mangelsyndromer
Andre undersøgelses-id-numre
- 41186-E/G
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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