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Comparison of Medication Adherence Between Once and Twice Daily Tacrolimus in Stable Renal Transplant Recipients

Comparison of Medication Adherence Between Once Daily Tacrolimus (Advagraf®) and Twice Daily Tacrolimus (Prograf®) Administration in Stable Renal Transplant Recipients - a Randomized Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01334333
Enrollment
46
Registered
2011-04-13
Start date
2011-11-11
Completion date
2018-03-01
Last updated
2018-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Renal Disease, Renal Transplant

Keywords

kidney transplant, tacrolimus, medication adherence, depression, neuropsychological, cognition, Self-efficacy, everyday problem solving

Brief summary

A critical aspect of real-world functioning following kidney transplantation involves how adherent individuals are to their medication regimens. Regardless of the possible dangers of failing to adhere to anti-rejection medications, such as increased graft rejection, studies have reported rates of non-adherence at almost 50% following renal transplant. The Cognitive Aging Laboratory under the direction of Dr. Wendy Thornton, at Simon Fraser University, has previously identified relationships between several potentially important cognitive and psychosocial variables, and self-reported medication adherence in renal transplant recipients, including depressive symptoms, as well as everyday and traditional cognitive functioning \[4\]. The possibility that changes in dosing regimens for a given medication may have an additional impact on medication adherence presents an important issue worth further exploration. The current study will allow for more thorough delineation of the roles of psychosocial and cognitive predictors of adherence with state-of-the-art monitoring techniques. In addition, the investigators will assess whether different dosing formulations of tacrolimus impact adherence behaviors in renal transplant recipients. The proposed research has two primary aims to examine: 1. To examine the role of cognitive and psychosocial variables in predicting medication adherence in renal transplant recipients. 2. To examine whether different formulations of tacrolimus (once per day dosing versus twice per day dosing) will impact medication adherence in renal transplant recipients.

Interventions

DRUGTacrolimus - Prograf® twice daily formulation

twice daily, dosage will be as determined by best treatment for each participant, duration of study period will be 4 months for each participant

DRUGTacrolimus - Advagraf® once daily formulation

once daily, dosage will be as determined by best treatment for each participant, duration of study period will be 4 months for each participant

Sponsors

Simon Fraser University
CollaboratorOTHER
Astellas Pharma Canada, Inc.
CollaboratorINDUSTRY
University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* a minimum of one year post renal transplant with a successful kidney graft and stable renal function (estimated glomerular filtration rate \[GFR (glomerular filtration rate)\] above 25 ml/minute per 1.73 m2). * currently prescribed tacrolimus * able to swallow pills * a minimum of grade six education * fluent in the English language.

Exclusion criteria

* refusal to or inability to give written informed consent. * any visual, hearing or other sensory/motor impairments which may interfere with the testing procedures. * have had a stroke determined to be of significant severity * have had a head injury determined to be of significant severity * have a current psychiatric diagnosis determined to be of significant severity * have the presence of an acute illness (e.g., metastatic cancer), neurological disease, and other major organ failure (e.g., end stage liver disease)

Design outcomes

Primary

MeasureTime frameDescription
electronic monitor of medication taking4 monthselectronic bottle tops will be used to monitor medication adherence using MEMS (medication event monitoring system) Caps technology for a period of 4 months.

Secondary

MeasureTime frameDescription
blood levels of medication4 monthsblood levels of tacrolimus will be monitored throughout the study.
self-reported medication adherence4 monthsself-report medication adherence questionnaires will also be used to assess medication adherence.
pharmacy refill data4 monthspharmacy refill data from the hospital pharmacy where all participants receive their medications will also be examined to determine medication adherence.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026