- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01359280
Nurse Delivered Cell Phone Adherence Intervention (Pick It UP) (PIU)
2. december 2014 opdateret af: Seth Kalichman, University of Connecticut
Nurse Delivered Cell Phone Adherence Intervention
Persistent adherence to antiretroviral therapy is necessary for the successful treatment of HIV infection.
The proposed research will test a theory-based behavioral intervention that includes objectively monitoring HIV treatment adherence with corrective feedback delivered by cell phone.
The study will also test the independent effects of an automated text message reminder system for sustaining adherence improvements.
The intervention under study has utility for people living with HIV/AIDS In resource limited rural and urban settings.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study is testing a theory-based HIV treatment adherence intervention delivered by cell phone to patients in urban and rural areas.
Adherence to antiretroviral (ART) medications is necessary to achieve HIV suppression and non-adherence can lead to treatment resistant genetic variants of HIV.
People living with HIV/AIDS often experience difficulty sustaining high-levels of treatment adherence.
Most factors that interfere with adherence are unanticipated and occur between clinical visits, including depression, side effects, substance use, and lapses in pharmacy refill.
We will conduct a randomized clinical trial to test a cell phone-delivered theory-based medication adherence counseling intervention.
The intervention is grounded in Self-Regulation Model and utilizes unannounced pill counts to monitor adherence and guide corrective feedback within the counseling context.
Using pill count adherence information for counseling allows providers to detect and correct patient non-adherence within a time frame that can head off viral resistance.
An experimental factorial design will test the effects of counseling and a text message reminder system as well the interaction of counseling and text message components with 600 men and women receiving HIV treatment.
Following screening, informed consent and baseline assessments participants will be randomized to one of four intervention conditions:(a) self-regulation counseling + regimen tailored text message reminders; (b) self-regulation counseling only; (c) control counseling + regimen tailored text reminders; or (d) control counseling only.
The study will therefore use a 2 (self-regulation counseling) x 2 (text message reminders) full factorial deign with participants followed for 9 months post-intervention.
The primary endpoints are medication adherence assessed by unannounced pill counts and HIV RNA (viral load).
This newly developed intervention strategy is grounded in Self-Regulation Theory and is designed for use in clinical settings with limited resources.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
600
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Connecticut
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Storrs, Connecticut, Forenede Stater, 06269
- University of Connecticut
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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 og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Age 18 or older
- Currently taking HIV treatment medication with non-adherence
Exclusion Criteria:
- Under age 18
- Not HIV positive
- Not taking HIV treatment medications
- Adherent to HIV Medications
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Faktoriel opgave
- Maskning: Tredobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Adherence Counseling + Text Messages
Participants receive one office-based adherence counseling session and 4 phone-delivered counseling sessions focused on antiretroviral adherence strategies using a model of behavioral self regulation skills building.
Participants also receive follow-up medication reminder text messages delivered by cell phone.
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5 Sessions of theory-based medication adherence counseling
Daily medication regimen tailored adherence reminders delivered by cell phone
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Eksperimentel: Adherence Counseling Only
Participants receive one office-based adherence counseling session and 4 phone-delivered counseling sessions focused on antiretroviral adherence strategies using a model of behavioral self regulation skills building.
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5 Sessions of theory-based medication adherence counseling
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Placebo komparator: General Health Counseling Only
Participants receive one office-based counseling session and 4 phone-delivered counseling sessions focused on general health and nutrition strategies using a model of behavioral self regulation skills building.
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5 sessions of health improvement counseling
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Placebo komparator: General Health Messages + Text Messages
Participants receive one office-based counseling session and 4 phone-delivered counseling sessions focused on general health and nutrition strategies using a model of behavioral self regulation skills building.
Participants also receive follow-up medication reminder text messages delivered by cell phone.
|
Daily medication regimen tailored adherence reminders delivered by cell phone
5 sessions of health improvement counseling
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Chart Abstracted Viral Load
Tidsramme: 12 months retrospective
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Patient HIV viral load is abstracted from medical records at baseline and at 12-month retrospective follow-up.
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12 months retrospective
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Unannounced Pill Count Adherence
Tidsramme: Monthly
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Unannounced phone-based pill counts conducted monthly to obtain an objective measure of medication adherence
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Monthly
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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: Seth C Kalichman, PhD, University of Connecticut
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. juli 2011
Primær færdiggørelse (Faktiske)
1. august 2014
Studieafslutning (Faktiske)
1. august 2014
Datoer for studieregistrering
Først indsendt
20. maj 2011
Først indsendt, der opfyldte QC-kriterier
20. maj 2011
Først opslået (Skøn)
24. maj 2011
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
3. december 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
2. december 2014
Sidst verificeret
1. december 2014
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- H10-332
- 1R01NR012962-01 (U.S. NIH-bevilling/kontrakt)
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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