- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01861210
Couples HIV Counseling and Testing for Male Couples in the United States (CVCT)
20. maj 2015 opdateret af: Patrick S Sullivan, Emory University
This is a study to determine whether testing for HIV together as a couple, as opposed to testing separately, in acceptable to men in male couples, and is a safe prevention service.
Testing of couples together has been provided for decades in Africa, but has never been tested in the United States.
In this study, male couples will be enrolled and randomly assigned to be tested together in the same room, or separately.
At the time of testing, investigators will ask questions about how they felt about the service they received.
Three months later, investigators will survey the men again, and determine whether they had any problems after the testing, like violence in the relationship or the relationship breaking up.
The main outcomes are being satisfied with the testing service, and safety (lack of intimate partner violence or relationship termination).
Although the study is not designed to determine if the service reduces risk behaviors for HIV transmission, investigators will examine data on risks just to explore that topic.
The main hypotheses are: (1) men will be at least as satisfied with couples testing as they are with individual testing; and (2) men tested as couples will not experience higher rates of intimate partner violence or relationship dissolution, relative to men tested separately.
Studieoversigt
Status
Afsluttet
Betingelser
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
216
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
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Georgia
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Atlanta, Georgia, Forenede Stater, 30309
- AID Atlanta
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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
18 år til 39 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Han
Beskrivelse
Inclusion Criteria:
- male at birth
- currently self-identify as male
- at least 18 years of age
- have been in a couple with a man for at least 3 months
- willing to complete a follow-up study visit in 3 months
- able to complete study assessments in English.
Exclusion Criteria:
- known to be HIV-positive
- over 39 years of age
- either partner being unwilling to accept randomization to the couples testing arm
- either partner planning to move from the Atlanta area within 3 months of the initial study visit
- either partner reporting a history of intimate partner violence
- either partner reporting feeling coerced to tested with his partner
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: Couples Counseling and Testing
Couples Voluntary HIV Counseling and Testing, adapted for use with male couples from the standard African couples testing service.
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Andre navne:
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Aktiv komparator: Individudal Counseling and Testing
Individual Voluntary Counseling and Testing involves HIV testing and individual, client-centered HIV prevention counseling.
This service is provided by counselors trained in Centers for Disease Control and Prevention's "Fundamentals of HIV Prevention Counseling" training.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Intimate partner violence
Tidsramme: 3 months
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Having been punched, hit, or kicked by the partner he tested with, injured to the point of feeling physical pain the day after a fight, or inflicting any of these acts on his partner in the preceding three months.
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3 months
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Relationship dissolution
Tidsramme: 3 months, or at the time of followup survey
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Either or both partners reported that the relationship ended after their participation in the study
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3 months, or at the time of followup survey
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Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Satisfaction with counseling service
Tidsramme: Within 30 minutes after the service
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Seven items asked on a 5-point Likert scale:
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Within 30 minutes after the service
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Patrick S Sullivan, PhD, Emory University Rollins School of Public Health
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. september 2010
Primær færdiggørelse (Faktiske)
1. maj 2012
Studieafslutning (Faktiske)
1. juni 2012
Datoer for studieregistrering
Først indsendt
21. maj 2013
Først indsendt, der opfyldte QC-kriterier
22. maj 2013
Først opslået (Skøn)
23. maj 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
22. maj 2015
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
20. maj 2015
Sidst verificeret
1. maj 2015
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- IRB00043714
- R34MH086331 (U.S. NIH-bevilling/kontrakt)
- CVCTMSM (Anden identifikator: Other)
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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