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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02639949
Other study ID # NIDDK_KUH
Secondary ID
Status Completed
Phase N/A
First received December 17, 2015
Last updated September 12, 2017
Start date January 2010
Est. completion date July 2017

Study information

Verified date September 2017
Source National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Nonadherence to medication is a major obstacle to successful treatment of renal transplant patients. This study has two primary aims. The first is to test whether a culturally sensitive cognitive-behavioral adherence promotion program could significantly improve medication adherence to tacrolimus prescription. Participants will be randomly assigned to either group CBT or to standard care. The second aim is to pilot a novel strategy of adherence measurement - unannounced telephone pill counts, which has been shown to be a valid and reliable means to measure medication adherence in other patient populations. Participants will be recruited from waiting area of the kidney transplant clinic at SUNY Downstate Medical Center in Brooklyn, NY. Three unannounced telephone pill counts will be conducted prior to start of the intervention in order to establish baseline adherence and three pill counts will be conducted post-intervention. Tacrolimus trough concentration levels will also be collected as an additional biological measure of adherence.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date July 2017
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- current prescription of tacrolimus less than 98% adherence to medication prescription as determined by three baseline pill counts

Exclusion Criteria:

- lack of telephone to complete pill counts lack of English proficiency to participate in adherence promotion sessions

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive-behavioral adherence promotion program
A culturally sensitive group cognitive behavioral therapy combined with adherence promotion.
Standard Care


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Outcome

Type Measure Description Time frame Safety issue
Primary Adherence as measured by unannounced telephone pill count 3 months
Secondary degree of agreement between pill count data and laboratory tacrolimus levels 3 months
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