- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02274844
Improving Medication Adherence in the Alabama Black Belt
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
Improving medication adherence is one of the greatest challenges in modern medicine. Despite decades of research on the topic, as many as half of patients with chronic diseases are not taking medications as recommended, and costs of nonadherence have been estimated at $290 billion annually. One reason for this persistent finding could be that interventions rarely acknowledge medications within the larger context of the lived experience of illness. Drawing on hundreds of patient interviews, Corbin and Strauss showed that chronic illness is a fundamentally destabilizing influence that forces us to confront the potential limitations of our "new", chronically ill self. Accepting our illness may be a crucial step in embracing medication adherence and other self-management behaviors as ways to restore balance following this disruption. The Corbin and Strauss framework is not often used to develop and test interventions to improve medication adherence, and this is the central objective of this proposal.
Medication adherence is especially critical in regions like rural Alabama, where residents have among the worst health outcomes in the US. Rates of cardiovascular mortality, diabetes and obesity are very high, but resources are scarce and the area's predominately black residents have deep-seated mistrust of the healthcare system (the region includes Tuskegee, site of the infamous syphilis study). This project was designed in collaboration with our community member partners and builds on a 5-year partnership of community-engaged research on diabetes peer coaching interventions and our experience with peer storytelling. The investigators will test the hypothesis that an intervention designed within the Corbin and Strauss framework can improve adherence and health outcomes compared to usual care. Our Aims are:
Aim 1: With our community partners, using qualitative research methods, build on already developed culturally tailored education material to develop the medication adherence intervention. The intervention will consist of educational DVDs with integrated storytelling about how community members accepted their disease and overcame barriers to medication adherence, plus one-on-one telephonic peer coaching. Activities include conducting focus groups with patients; creating the DVDs and the coaching intervention protocol; training peer coaches; and pilot testing.
Aim 2: Conduct a randomized controlled trial with 500 individuals with type 2 diabetes and medication nonadherence. The trial will compare the effect of usual care and the intervention on medication adherence and physiologic risk factors including A1c, blood pressure and low density lipoprotein cholesterol (primary outcomes), and quality of life and self-efficacy (secondary outcomes).
This innovative approach would be a major shift in how patients are helped in under resourced areas living with chronic diseases commit to taking medications, improving health and eventually reducing health disparities.
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Alabama
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Birmingham, Alabama, Stati Uniti, 35210
- Univeristy of Alabama at Birmingham
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- adults
- type 2 diabetes
- taking medications for diabetes
- medication non adherent
Exclusion Criteria:
- nursing home residence
- plans to move away in the next year
- advanced illnesses such as hemodialysis, cancer or dementia
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: Peer Coaching
The intervention participants will receive the Living Well with Diabetes Program.
The program will consist of educational DVDs with integrated storytelling about how community members accepted their disease and overcame barriers to medication adherence, plus one-on-one telephonic peer coaching.
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The intervention participants will receive the Living Well with Diabetes Program.
The program will consist of educational DVDs with integrated storytelling about how community members accepted their disease and overcame barriers to medication adherence, plus one-on-one telephonic peer coaching
|
|
Nessun intervento: Usual Care
At enrollment, the investigators will provide an educational DVD on general health and wellness topics including vaccination, cancer screening, osteoporosis and other topics not related to diabetes care.
There will be no peer storytelling on these DVDs.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in Self Reported Medication Adherence
Lasso di tempo: Baseline, 6 months
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Patient-reported adherence to medications as a medication adherence score, from 0-3, where a higher score indicates worse adherence.
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Baseline, 6 months
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Change in Percentage of HbA1c
Lasso di tempo: Baseline, 6 months
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Hemoglobin A1c test to identify the average amount of glucose (sugar) present in a patient's blood.
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Baseline, 6 months
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Change in Blood Pressure
Lasso di tempo: Baseline, 6 months
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2 BP measures were taken 1 minute apart using a LifeSource UA-789 digital blood pressure monitor.
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Baseline, 6 months
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Change in Low-Density Lipoprotein (LDL) Cholesterol
Lasso di tempo: Baseline, 6 months
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Finger stick, spectrophotometer to measure cholesterol level.
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Baseline, 6 months
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Change in Quality of Life as Assessed With the Short Form 12- Mental Component
Lasso di tempo: Baseline, 6 months
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Short Form-12 Mental Component and Physical Component Summary scores range from 0-100; higher scores indicate greater quality of life.
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Baseline, 6 months
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Change in Quality of Life as Assessed With the Short Form-12- Physical Component
Lasso di tempo: Baseline, 6 months
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Short Form-12 Mental Component and Physical Component Summary scores range from 0-100; higher scores indicate greater quality of life.
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Baseline, 6 months
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Change in Medication Use Self-efficacy Score as Measured by SEAMS Scale and the Perceived Diabetes Self-Management Scale, Which is Associated With A1c
Lasso di tempo: Baseline, 6 months
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Medication use self-efficacy scores for range from 13-39; higher scores indicate higher levels of self-efficacy for medication adherence.
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Baseline, 6 months
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Change in Diabetes-Specific Quality of Life
Lasso di tempo: Baseline, 6 months
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Diabetes specific quality of life will be assessed using the validated Diabetes Distress Scale.The DDS is a 17-item instrument that measures diabetes-related emotional distress.
Participants rate the degree to which each item is problematic for them on a 6-point Likert scale, from 1 (no problem) to 6 (serious problem).
A score of 3 or greater = moderate distress.
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Baseline, 6 months
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Number of Physician Office Visits 6 Months
Lasso di tempo: 6 months
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6 months
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Number of Hospital Stays at 6 Months
Lasso di tempo: 6 months
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6 months
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Number of Emergency Visits at 6 Months
Lasso di tempo: 6 months
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6 months
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Change in Diabetes Medication Counts
Lasso di tempo: Baseline, 6 months
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Change in number of diabetes medications.
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Baseline, 6 months
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in Medication Beliefs- Harm (Beliefs That Medications Are Harmful)
Lasso di tempo: Baseline, 6 months
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Beliefs about medications questionnaire scores range from 5-25; higher scores indicate stronger beliefs.
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Baseline, 6 months
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Change in Medication Beliefs- Overuse (Concerns About the Way Doctors Use Medications)
Lasso di tempo: Baseline, 6 months
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Beliefs about medications questionnaire scores range from 5-25; higher scores indicate stronger beliefs.
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Baseline, 6 months
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Change in Medication Beliefs-Necessity (Beliefs About the Necessity of Medications)
Lasso di tempo: Baseline, 6 months
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Beliefs about medications questionnaire scores range from 5-25; higher scores indicate stronger beliefs.
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Baseline, 6 months
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Change in Medication Beliefs- Concerns (Concerns About the Negative Effects of Medications)
Lasso di tempo: Baseline, 6 months
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Beliefs about medications questionnaire scores range from 5-25; higher scores indicate stronger beliefs.
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Baseline, 6 months
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Collaboratori e investigatori
Investigatori
- Investigatore principale: Monika M Safford, MD, Weill Medical College of Cornell University
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Inizio studio (Effettivo)
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Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- PCORI-R-AD-1306-03565
Piano per i dati dei singoli partecipanti (IPD)
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Descrizione del piano IPD
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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