Self-Management Assistance for Recommended Treatment (SMART) Portal (SMART)
18 juli 2017 uppdaterad av: Children's Hospital Medical Center, Cincinnati
The purpose of the study is to develop, evaluate, and optimize an interactive website (the SMART portal).
The SMART portal will use IBD-specific and general assessments and interventions to reduce the burden of common barriers to treatment adherence and enhance self-management skills.
This study aims to build and revise the SMART portal according to feedback and testing from participants.
Studieöversikt
Status
Avslutad
Detaljerad beskrivning
The study consists of three phases for development and evaluation of the SMART portal.
Phase 1 is the development of online assessments and intervention components.
There will be no participant interaction with the portal during Phase 1. Phase 2 will consist of one, individual interview with patients, caregivers, and clinicians/nurses to interact with a portal prototype and provide feedback.
Phase 3 will contain an open trial for patients and caregivers with baseline, 2-6 months interacting with the portal and progressing through applicable intervention components, and post-treatment.
Patient test data will also be loaded into the portal during Phase 3 for clinicians/nurses to interact with for 2-6 months.
Feedback from all users will be collected at post-treatment for optimization of the portal.
Studietyp
Observationell
Inskrivning (Faktisk)
87
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Ohio
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Cincinnati, Ohio, Förenta staterna, 45229
- Cincinnati Children's Hospital Medical Center
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Virginia
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Charlottesville, Virginia, Förenta staterna, 22901
- BeHealth Solutions, LLC
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
11 år till 18 år (Barn, Vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Testmetod
Icke-sannolikhetsprov
Studera befolkning
Patients, caregivers, clinicians, and nurses will be recruited from the IBD clinic at Cincinnati Children's Hospital Medical Center.
Beskrivning
Inclusion Criteria:
- Patient diagnosed with Crohn's disease, ulcerative colitis, or indeterminate colitis (collectively known as IBD)
- Patient between 11 and 18 years of age
- Patient prescribed at least one oral medication used to treat IBD
- Access to the internet whether public (example, library) or private (example, home, personal)
- English fluency for patient, caregiver, and clinician/nurse
- Clinician/nurse currently providing medical treatment to patients diagnosed with IBD through the IBD Center at Cincinnati Children's Hospital Medical Center
Exclusion Criteria:
- Diagnosis of pervasive developmental disorder in patient or caregiver
- Diagnosis of serious mental illness (example, schizophrenia) in patient or caregiver
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
Kohorter och interventioner
Grupp / Kohort |
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Clinicians/Nurses
Clinicians and nurses who treat patients diagnosed with IBD will be recruited to interact with and use the SMART portal to provide feedback on optimization.
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Patients
Patients age 11-18 years diagnosed with IBD will be recruited to interact with and use the SMART portal to provide feedback on optimization.
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Caregivers
Caregivers of patients diagnosed with IBD will be recruited to interact with and use the SMART portal to provide feedback on optimization.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Medication adherence
Tidsram: Phase 3 - Approximately 2-6 months, depending upon progression through portal components
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Medication adherence will be measured by pill count data provided by patients or caregivers at baseline and post-treatment during Phase 3. Phase 3 will start approximately in October 2014 and continue through March 2015.
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Phase 3 - Approximately 2-6 months, depending upon progression through portal components
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Disease severity
Tidsram: Phase 3 - Approximately 2-6 months, depending upon progression through portal components
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Disease severity will be measured at baseline, post-treatment, and periodically throughout the intervention as the patient logs in to view intervention materials during Phase 3. The portal will prompt the patient to complete disease severity questions throughout the intervention, but it will be dependent upon the patient actually logging into the system.
Therefore, exact time points during treatment are unknown.
The Pediatric Ulcerative Colitis Activity Index (PUCAI) will be used to measure disease severity for patients diagnosed with ulcerative colitis and indeterminate colitis, and the Partial Harvey Bradshaw (PHBI) will be used for patients diagnosed with Crohn's disease.
Phase 3 will start approximately in October 2014 and continue through March 2015.
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Phase 3 - Approximately 2-6 months, depending upon progression through portal components
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Health-related quality of life
Tidsram: Phase 3 - Approximately 2-6 months, depending upon progression through portal components
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The IMPACT-III will be used during baseline and post-treatment in Phase 3 to measure quality of life in patients.
Phase 3 will start approximately in October 2014 and continue through March 2015.
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Phase 3 - Approximately 2-6 months, depending upon progression through portal components
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Samarbetspartners
Utredare
- Studiestol: Lee Denson, M.D., Children's Hospital Medical Center, Cincinnati
- Studiestol: James Peugh, Ph.D., Children's Hospital Medical Center, Cincinnati
- Studiestol: Korey Hood, Ph.D., University of California, San Francisco
- Studiestol: Lee Ritterband, Ph.D., BeHealth Solutions, LLC.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 juli 2013
Primärt slutförande (Faktisk)
1 juni 2016
Avslutad studie (Faktisk)
1 juni 2016
Studieregistreringsdatum
Först inskickad
4 oktober 2013
Först inskickad som uppfyllde QC-kriterierna
17 oktober 2013
Första postat (Uppskatta)
22 oktober 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
19 juli 2017
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
18 juli 2017
Senast verifierad
1 juli 2017
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- SMART
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