- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01359280
Nurse Delivered Cell Phone Adherence Intervention (Pick It UP) (PIU)
2. desember 2014 oppdatert av: 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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Detaljert 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.
Studietype
Intervensjonell
Registrering (Faktiske)
600
Fase
- Fase 2
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
Connecticut
-
Storrs, Connecticut, Forente stater, 06269
- University of Connecticut
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år og eldre (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
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
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Faktoriell oppgave
- Masking: Trippel
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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.
|
5 Sessions of theory-based medication adherence counseling
Daily medication regimen tailored adherence reminders delivered by cell phone
|
|
Eksperimentell: 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.
|
5 Sessions of theory-based medication adherence counseling
|
|
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.
|
5 sessions of health improvement counseling
|
|
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
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Chart Abstracted Viral Load
Tidsramme: 12 months retrospective
|
Patient HIV viral load is abstracted from medical records at baseline and at 12-month retrospective follow-up.
|
12 months retrospective
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Unannounced Pill Count Adherence
Tidsramme: Monthly
|
Unannounced phone-based pill counts conducted monthly to obtain an objective measure of medication adherence
|
Monthly
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Seth C Kalichman, PhD, University of Connecticut
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. juli 2011
Primær fullføring (Faktiske)
1. august 2014
Studiet fullført (Faktiske)
1. august 2014
Datoer for studieregistrering
Først innsendt
20. mai 2011
Først innsendt som oppfylte QC-kriteriene
20. mai 2011
Først lagt ut (Anslag)
24. mai 2011
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
3. desember 2014
Siste oppdatering sendt inn som oppfylte QC-kriteriene
2. desember 2014
Sist bekreftet
1. desember 2014
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- H10-332
- 1R01NR012962-01 (U.S. NIH-stipend/kontrakt)
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .