TY - JOUR
T1 - Determining the primary endpoint for a stimulant abuse trial
T2 - Lessons learned from STRIDE (CTN 0037)
AU - Trivedi, Madhukar H.
AU - Greer, Tracy L.
AU - Potter, Jennifer Sharpe
AU - Grannemann, Bruce D.
AU - Nunes, Edward V.
AU - Rethorst, Chad
AU - Warden, Diane
AU - Ring, Kolette M.
AU - Somoza, Eugene
N1 - Funding Information:
Dr. J.S. Potter and Dr. E.V. Nunes have received funding from NIDA.
Funding Information:
Dr. T.L. Greer has received funding from NARSAD and an award from NIH.
Funding Information:
Dr. D. Warden has owned stock in Pfizer, Inc., and Bristol Meyers Squibb in the past 5 years and has received funding from NARSAD.
Funding Information:
This work is supported by the National Institute of Drug Abuse through the Clinical Trials Network for the Stimulant Reduction Intervention using Dosed Exercise (STRIDE) study (U10 DA 02002405S2) PIs: B. Adinoff and M.H. Trivedi; Lead Investigator: M.H. Trivedi; NIDA K24 DA022412 (PI: E. Nunes); and NIDA U10 DA13035 (PI: E. Nunes).
PY - 2011/9
Y1 - 2011/9
N2 - Background: No consensus is available for identifying the best primary outcome for substance use disorder trials, making interpretation across trials difficult. Abstinence is the most desirable treatment outcome although a wide variety of other endpoints have been used. Objectives: This report provides a framework for determining an optimal primary endpoint and the relevant measurement approach for substance use disorder treatment trials. The framework was developed based on a trial for stimulant abuse using exercise as an augmentation treatment, delivered within the NIDA Clinical Trials Network. The use of a common endpoint across trials will facilitate comparisons of treatment efficacy. Methods: Primary endpoint options in existing substance abuse studies were evaluated. This evaluation included surveys of the literature for endpoints and measurement approaches, followed by assessment of endpoint choices against study design issues, population characteristics, tests of sensitivity, and tests of clinical meaningfulness. Conclusion: We concluded that the best current choice for a primary endpoint is percent days abstinent, as measured by the Time Line Follow Back interview conducted three times a week with recall aided by a take-home Substance Use Diary. To improve the accuracy of the self-reported drug use, the results of qualitative urine drug screens will be used in conjunction with the Time Line Follow Back results. Scientific Significance: There is a need for a standardized endpoint in this field to allow for comparison across treatment studies, and we suggest that the recommended candidate endpoint be considered. However, the study design and goals ultimately must guide the final decision.
AB - Background: No consensus is available for identifying the best primary outcome for substance use disorder trials, making interpretation across trials difficult. Abstinence is the most desirable treatment outcome although a wide variety of other endpoints have been used. Objectives: This report provides a framework for determining an optimal primary endpoint and the relevant measurement approach for substance use disorder treatment trials. The framework was developed based on a trial for stimulant abuse using exercise as an augmentation treatment, delivered within the NIDA Clinical Trials Network. The use of a common endpoint across trials will facilitate comparisons of treatment efficacy. Methods: Primary endpoint options in existing substance abuse studies were evaluated. This evaluation included surveys of the literature for endpoints and measurement approaches, followed by assessment of endpoint choices against study design issues, population characteristics, tests of sensitivity, and tests of clinical meaningfulness. Conclusion: We concluded that the best current choice for a primary endpoint is percent days abstinent, as measured by the Time Line Follow Back interview conducted three times a week with recall aided by a take-home Substance Use Diary. To improve the accuracy of the self-reported drug use, the results of qualitative urine drug screens will be used in conjunction with the Time Line Follow Back results. Scientific Significance: There is a need for a standardized endpoint in this field to allow for comparison across treatment studies, and we suggest that the recommended candidate endpoint be considered. However, the study design and goals ultimately must guide the final decision.
KW - Cocaine abuse
KW - Endpoint
KW - Exercise
KW - Measurement
KW - Stimulant abuse
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U2 - 10.3109/00952990.2011.598589
DO - 10.3109/00952990.2011.598589
M3 - Article
C2 - 21854276
AN - SCOPUS:80052235784
SN - 0095-2990
VL - 37
SP - 339
EP - 349
JO - American Journal of Drug and Alcohol Abuse
JF - American Journal of Drug and Alcohol Abuse
IS - 5
ER -