- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00686049
HIV Treatment-Readiness Measure (HTRM) Validation
Validation of the HIV Treatment Readiness Measure (HTRM)
The goal of this study is to assess the reliability of the HIV
Treatment Readiness Measure (HTRM) to assist clinicians in:
(1) determining whether or not youth living with HIV are ready to initiate HAART and (2) identifying youth who may be in need of additional support services to facilitate their adherence to HAART. The current study will examine the psychometric properties of the HTRM and establish its test-retest reliability over a two week period. If the HTRM is found to be reliable, a subsequent study will examine its predictive validity.
Studieöversikt
Status
Betingelser
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
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California
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Los Angeles, California, Förenta staterna, 90027
- Childrens Hospital of Los Angeles
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San Francisco, California, Förenta staterna, 94117
- University of California San Francisco
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District of Columbia
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Washington, District of Columbia, Förenta staterna, 20010-2970
- Childrens National Medical Center
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Florida
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Fort Lauderdale, Florida, Förenta staterna, 33316
- Childrens Diagnostic & Treatment Center, Inc
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Miami, Florida, Förenta staterna, 33101
- University of Miami School of Medicine
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Tampa, Florida, Förenta staterna, 33606
- USF College of Medicine
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Illinois
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Chicago, Illinois, Förenta staterna, 60614
- Childrens Memorial Hospital
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Chicago, Illinois, Förenta staterna, 60612
- Ruth M Rothstein CORE Center/ John H Stroger Jr Hospital
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Louisiana
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New Orleans, Louisiana, Förenta staterna, 70112
- Tulane University Health Sciences Center
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Maryland
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Baltimore, Maryland, Förenta staterna, 21201
- University of Maryland Express Mailing Address:
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New York
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Bronx, New York, Förenta staterna, 10467
- Montefiore Medical Center
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New York, New York, Förenta staterna, 10128
- Mount Sinai Medical Center
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Pennsylvania
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Philadelphia, Pennsylvania, Förenta staterna, 19104
- The Childrens Hospital of Philadelphia
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Tennessee
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Memphis, Tennessee, Förenta staterna, 38105-3678
- St Jude Childrens Research Hospital
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-
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San Juan, Puerto Rico, 00936-5067
- University of Puerto Rico, Medical Sciences Campus
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
Inclusion Criteria:
- HIV-positive youth, 13 years 0 days to 24 years 364 days of age
- Either HAART naïve (defined as never having taken HAART) or HAART experienced (defined as having had at least one experience taking HAART and not having taken HAART for 30 days prior to study entry)
- Not currently on HAART, but planning to initiate HAART within the next 2 months based on provider recommendation
- Enrolled in care at an AMTU or a collaborating site
- Able to speak and understand English
- Willing to provide informed consent, or assent with parental permission (if required by the site IRB) for participation in this study.
Exclusion Criteria:
- Evidence of cognitive impairment or other mental condition that limits his/her ability to complete the assessment (per PI or designee discretion)
- Determined by the PI (or designee) to be under the influence of psychoactive agents or intoxicated at the time of assessment to a degree that would interfere with successful completion of the questionnaire
- Visibly distraught or unstable
- Any clinical condition that would likely interfere with the participant's ability to complete the study
Participants who are unable to speak English will be excluded from the initial testing of the HTRM's reliability and validity in keeping with traditional tool development strategies. If the initial study indicates that the English version of the HTRM is reliable and valid, appropriate methods will be employed to translate the instrument into Spanish and the reliability and validity will be re-examined for the Spanish version.
Studieplan
Hur är studien utformad?
Designdetaljer
- Observationsmodeller: Kohort
- Tidsperspektiv: Blivande
Kohorter och interventioner
Grupp / Kohort |
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Study Group
Participants will complete two audio computer assisted self interviews on laptop computers.
This study will also involve the abstraction of participants' viral load and CD4 counts from their medical charts.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
---|---|
To examine the factor structure and estimate the internal consistency of each factor of the HTRM.
Tidsram: 1 year
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1 year
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To estimate the test-retest reliability of the HTRM.
Tidsram: Entry, Week 2
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Entry, Week 2
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Sekundära resultatmått
Resultatmått |
Tidsram |
---|---|
To determine an appropriate system for scoring the HTRM.
Tidsram: 1 year
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1 year
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To examine the acceptability of the HTRM.
Tidsram: Entry, Week 2
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Entry, Week 2
|
Samarbetspartners och utredare
Samarbetspartners
Utredare
- Studiestol: M. Isabel Fernández, Ph.D., Adolescent Trials Network
Publikationer och användbara länkar
Användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- ATN 065
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