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

Primary Purpose

Renal Disease, Renal Transplant

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Tacrolimus - Prograf® twice daily formulation
Tacrolimus - Advagraf® once daily formulation
Sponsored by
University of British Columbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Renal Disease focused on measuring kidney transplant, tacrolimus, medication adherence, depression, neuropsychological, cognition, Self-efficacy, everyday problem solving

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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)

Sites / Locations

  • Solid Organ Transplant Clinic, Vancouver General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Prograf®

Advagraf®

Arm Description

Prograf® is a twice daily formulation of tacrolimus

Advagraf® is a once daily formulation of tacrolimus

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

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

Full Information

First Posted
April 11, 2011
Last Updated
May 14, 2018
Sponsor
University of British Columbia
Collaborators
Simon Fraser University, Astellas Pharma Canada, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01334333
Brief Title
Comparison of Medication Adherence Between Once and Twice Daily Tacrolimus in Stable Renal Transplant Recipients
Official Title
Comparison of Medication Adherence Between Once Daily Tacrolimus (Advagraf®) and Twice Daily Tacrolimus (Prograf®) Administration in Stable Renal Transplant Recipients - a Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
November 11, 2011 (Actual)
Primary Completion Date
October 30, 2014 (Actual)
Study Completion Date
March 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia
Collaborators
Simon Fraser University, Astellas Pharma Canada, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

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: To examine the role of cognitive and psychosocial variables in predicting medication adherence in renal transplant recipients. To examine whether different formulations of tacrolimus (once per day dosing versus twice per day dosing) will impact medication adherence in renal transplant recipients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Disease, Renal Transplant
Keywords
kidney transplant, tacrolimus, medication adherence, depression, neuropsychological, cognition, Self-efficacy, everyday problem solving

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Prograf®
Arm Type
Active Comparator
Arm Description
Prograf® is a twice daily formulation of tacrolimus
Arm Title
Advagraf®
Arm Type
Experimental
Arm Description
Advagraf® is a once daily formulation of tacrolimus
Intervention Type
Drug
Intervention Name(s)
Tacrolimus - Prograf® twice daily formulation
Other Intervention Name(s)
Prograf®
Intervention Description
twice daily, dosage will be as determined by best treatment for each participant, duration of study period will be 4 months for each participant
Intervention Type
Drug
Intervention Name(s)
Tacrolimus - Advagraf® once daily formulation
Other Intervention Name(s)
Advagraf®
Intervention Description
once daily, dosage will be as determined by best treatment for each participant, duration of study period will be 4 months for each participant
Primary Outcome Measure Information:
Title
electronic monitor of medication taking
Description
electronic bottle tops will be used to monitor medication adherence using MEMS (medication event monitoring system) Caps technology for a period of 4 months.
Time Frame
4 months
Secondary Outcome Measure Information:
Title
blood levels of medication
Description
blood levels of tacrolimus will be monitored throughout the study.
Time Frame
4 months
Title
self-reported medication adherence
Description
self-report medication adherence questionnaires will also be used to assess medication adherence.
Time Frame
4 months
Title
pharmacy refill data
Description
pharmacy refill data from the hospital pharmacy where all participants receive their medications will also be examined to determine medication adherence.
Time Frame
4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
R. Jean Shapiro, M.D.
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Wendy Loken Thornton, Ph.D.
Organizational Affiliation
Simon Fraser University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nilufar Partovi, Pharm.D.
Organizational Affiliation
University of British Columbia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Theone SE Paterson, M.A.
Organizational Affiliation
Simon Fraser University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Solid Organ Transplant Clinic, Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
36094829
Citation
Mellon L, Doyle F, Hickey A, Ward KD, de Freitas DG, McCormick PA, O'Connell O, Conlon P. Interventions for increasing immunosuppressant medication adherence in solid organ transplant recipients. Cochrane Database Syst Rev. 2022 Sep 12;9(9):CD012854. doi: 10.1002/14651858.CD012854.pub2.
Results Reference
derived
PubMed Identifier
31452902
Citation
Paterson TSE, Demian M, Shapiro RJ, Loken Thornton W. Impact of Once- Versus Twice-Daily Tacrolimus Dosing on Medication Adherence in Stable Renal Transplant Recipients: A Canadian Single-Center Randomized Controlled Trial. Can J Kidney Health Dis. 2019 Aug 17;6:2054358119867993. doi: 10.1177/2054358119867993. eCollection 2019.
Results Reference
derived

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

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