Kidney Disease Clinical Trial
Official title:
SystemCHANGE: An Intervention for Medication Adherence in Transplant Recipients
With kidney transplant (KT) recipients as our exemplar population, our goal is to develop and test interventions that increase medication adherence (MA) in chronically ill adults. Among adult KT recipients, non-adherence to immunosuppressive medications (MNA) is the leading predictor of poor outcomes, including rejection, kidney loss, and death. An alarming one-third of KT patients experience MNA even though the problem is preventable. Adherence intervention studies have proven marginally effective for those with acute and chronic illnesses and ineffective for adult KT recipients. Using a randomized controlled trial design with an attention-control group, this R01 will test an innovative 6-month SystemCHANGE intervention to enhance immunosuppressive MA in adult non-adherent KT recipients. This intervention shows great promise for increasing MA with a large effect size of 1.4 in our pilot study. Grounded in the socio-ecological model, SystemCHANGE seeks to systematically improve MA behaviors by identifying and shaping routines, involving supportive others in routines, and using medication taking feedback through small patient-lead experiments to change and maintain behavior. The Medication Event Monitoring System cap, which contains microelectronics that record the date and time of the cap removal, will be used to measure MA. Persistence of the MA behavior change will be examined by evaluating the difference in MA between the two groups during the 6-month maintenance phase. Mediators and moderators of MA will be examined. Health outcomes will be compared and a cost-effectiveness analysis will be conducted.
SPECIFIC AIMS For adult kidney transplant (KT) patients, the leading predictor of rejection,
kidney loss, death and their attendant costs is immunosuppressive medications nonadherence
(MNA). An alarming one-third of KT recipients experience this preventable problem. According
to meta-analysis, predictors of MNA are nonwhite ethnicity, poorer social support and poorer
perceived health. Patients' most frequent barrier to adhering to immunosuppressive medication
is forgetting. 9 Even minor deviations from adherence have shown negative effects, though the
precise extent of poor outcomes stemming from nonadherence is not clear. Traditionally,
intervention studies aimed at boosting adherence target cognition (knowledge, attitudes,
beliefs) and behavioral skills. However, these have proven marginally effective for
individuals with acute and chronic illnesses and ineffective for adult KT recipients. In a
sample of KT recipients, we propose to test the innovative and successful SystemCHANGE
intervention, which is grounded in the socio-ecological model. This approach is a paradigm
shift in behavioral interventions because it seeks to redesign the system of the
interpersonal environment and daily routines linked to health behavior, rather than to alter
individuals' efforts to change their behavior. Using a four-pronged, patient-centered
approach, we will (1) assess individual systems (including important others who shape
medication taking), how they influence medication taking and their proposals for improving
medication adherence, (2) implement the proposed individual systems solutions for improving
adherence, (3) track adherence data, and (4) evaluate adherence data through small
experiments. In our pilot study, this intervention yielded a large effect size of 1.4.
This study's innovation lies in its use of a socio-ecological model known as SystemCHANGE,
which differs greatly from previous cognitive and behavioral skills-focused interventions for
improving medication adherence. This will be the first rigorous evaluation of SystemCHANGE
with a diverse sample of KT recipients and long-term follow up. This study presents a unique
opportunity to evaluate moderators and mediators of adherence and has potential, based upon
pilot work, to have immediate "dose" impact. As such, it could hold great promise as an
intervention that translates very well into practice settings. Our 6-month SystemCHANGE
intervention (also referred to as "intervention") seeks to enhance adherence to
immunosuppressive medication among adult KT recipients who are non-adherent. The study is a
randomized controlled trial with an attention-control intervention (also referred to as
"control") to determine persistence of medication adherence behavior change and differences
in adherence between the two groups during the 6-month maintenance phase.
Primary Aim (PA):
PA: To determine whether the intervention is more effective than control in increasing
medication adherence in adult KT recipients at the completion of the intervention and
maintenance phases.
Hypothesis: Adult KT recipients participating in the intervention will have higher
immunosuppressive adherence rates than those participating in the control at the completion
of intervention and maintenance phases.
Secondary Aim (Sec):
SA: To examine the patterns of medication adherence in adult KT recipients in both groups.
Research question (RQ): When does the intervention become effective (e.g., what "dose" is
needed)? RQ: What is the pattern of decay in adherence over time in both groups?
Exploratory Aims (EA):
EA1: To determine whether the intervention is more effective than the control in decreasing
poor health outcomes (e.g. increasing creatinine/BUN, infection, acute/chronic rejection,
graft loss, death, hospitalizations, length of hospital stay, and healthcare appointments).
Hypothesis: At one year, there will be differential levels of poor outcomes, with the
intervention demonstrating lower levels of poor outcomes than the control.
EA2: To evaluate the role of potential mediators and moderators of medication adherence and
health outcomes in adult KT recipients in the intervention and those in the control.
Hypothesis: Incorporating potential mediators and moderators of the intervention (e.g.,
nonwhite ethnicity, perceived social support, perceived health status, personal systems
behavior) will increase the medication adherence variance explained by the intervention.
EA3: To determine if the intervention is cost-effective. Hypothesis: The cost-effectiveness
ratio for the intervention will be less than for the control.
Each year, 35.6 KT recipients per 100 are non-adherent with their medications, which is the
primary cause of post-transplant morbidity. Thus, the need for effective interventions is
compelling: Decreasing transplant complications from MNA will reduce costs and make
additional kidneys available to those waiting for transplants by reducing the number of KT
recipients who must rejoin the organ list. This project builds on our research team's
previous adherence work, including a SystemCHANGE intervention pilot study that addresses
Healthy People 2020 initiatives of reducing chronic kidney disease complications, disability,
death, and costs by optimizing transplant medication adherence and increasing the number of
patients who receive a transplant.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02369354 -
Transplant Social Worker Support for Live Kidney Donation in African Americans
|
N/A | |
Not yet recruiting |
NCT02225782 -
Trial to Compare 1.0 Versus 2.0 mg Alteplase (tPA) Dosing in Restoring Hemodialysis Catheter Function
|
Phase 4 | |
Completed |
NCT00499187 -
Fanconi Syndrome Due to ARVs in HIV-Infected Persons
|
Phase 4 | |
Withdrawn |
NCT00585429 -
Evaluation of Kidney Disease in Liver Transplant Recipients
|
N/A | |
Completed |
NCT00379899 -
ADVANCE: Study to Evaluate Cinacalcet Plus Low Dose Vitamin D on Vascular Calcification in Subjects With Chronic Kidney Disease Receiving Hemodialysis
|
Phase 4 | |
Completed |
NCT00183248 -
Using Donor Stem Cells and Alemtuzumab to Prevent Organ Rejection in Kidney Transplant Patients
|
Phase 1/Phase 2 | |
Completed |
NCT00001835 -
Oxaliplatin in Cancer Patients With Impaired Kidney Function
|
Phase 1 | |
Completed |
NCT01331941 -
A Pharmacokinetic Study of AMG 386 in Cancer Subjects With Normal and Impaired Renal Function
|
Phase 1 | |
Terminated |
NCT00436748 -
Study to Assess Darbepoetin Alfa Dosing for the Correction of Anemia in Pediatric Patients With Chronic Kidney Disease
|
Phase 3 | |
Completed |
NCT01467466 -
Prevention of Serious Adverse Events Following Angiography
|
Phase 3 | |
Completed |
NCT01235936 -
Safety and Efficacy Study for AKB-6548 in Participants With Chronic Kidney Disease and Anemia
|
Phase 2 | |
Completed |
NCT01974999 -
A Retrospective Multicenter Study to Determine 5-Year Clinical Outcomes in Subjects Previously Enrolled in the CTOT-01 Study
|
||
Completed |
NCT01947829 -
Interdialytic Kt/V Variability Measurement With Adimea (IVP STUDY)
|
N/A | |
Recruiting |
NCT01240564 -
The Nephrotic Syndrome Study Network (NEPTUNE)
|
N/A | |
Active, not recruiting |
NCT01228903 -
Uric Acid and the Endothelium is CKD
|
N/A | |
Completed |
NCT00734357 -
Comparative Investigation of Intravenously Administered Omnipaque and Isovue: Effects on Serum Creatinine Concentration in Outpatients
|
N/A | |
Completed |
NCT00781417 -
Prevention of Secondary Hyperparathyroidism With Vitamin D in Stage II/III Chronic Kidney Disease
|
N/A | |
Completed |
NCT00093977 -
Study to Assess Darbepoetin Alfa in Subjects With Chronic Kidney Disease
|
Phase 3 | |
Completed |
NCT00094484 -
Cinacalcet HCl in Chronic Kidney Disease Subjects With Secondary Hyperparathyroidism Not Receiving Dialysis
|
Phase 3 | |
Completed |
NCT00185159 -
Olmesartan Medoxomil in Diabetes Mellitus
|
Phase 3 |