Architecture Design of Generic Outcome Adjudication in CTMS Wenle Zhao, PhD Medical University of South Carolina, Charleston, SC, 29425, USA Society for.

Slides:



Advertisements
Similar presentations
Fundamentals of Clinical Trials
Advertisements

Safety Reporting IN Clinical Trials
2014 Supplemental Forms: Automation Instructions.
New Trials If you are seeking a collaboration with the UCL CCTU we require you to apply: At least 3 months before the application deadline By using the.
ADVERSE EVENT REPORTING
Adverse Event Reporting. Reporting Adverse Events Adverse Events (AEs) are “... any untoward medical occurrence in a subject that was not previously identified.
CRC Protocol Documents Protocol Submissions Amendments Publications Study Closure.
Capturing and Reporting Adverse Events in Clinical Research
Neurological Emergencies Treatment Trials SAEM 2006.
RAMPART Statistical Analysis Plan Valerie Durkalski NETT Statistical and Data Management Center Department of Biostatistics, Bioinformatics & Epidemiology.
Using EDC-Rave to Conduct Clinical Trials at Genentech
Medical School Preparation for LCME Accreditation The University Toledo College of Medicine August 24, 2011 Barbara Barzansky, PhD, MHPE LCME Secretary,
Coordinator University Clinical Research Pharmacy Investigational Drug Service (IDS) Marjorie Shaw Phillips, MS, RPh, FASHP Clinical Research Pharmacist.
CALGB Informational Session June 22, 2007 David Hurd, MD Interim Chair Data Audit Committee.
NCI Clinical Trials Reporting Program CTRP User Meeting May 2, 2012 Gene Kraus CTRP Program Director.
Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial Adverse Event Reporting Catherine Dillon.
ACRIN 6698 Diffusion-weighted MRI Biomarkers for Assessment of Breast Cancer Response to Neoadjuvant Treatment: An I-SPY 2 Trial Substudy Presented by:
Ron Sokol, M.D. Principal Investigator, CCTSI Bonnie Walters Executive Director, The Evaluation Center Kathryn Nearing, Ph.D. Associate Director, The Evaluation.
Adverse Events, Unanticipated Problems, Protocol Deviations & other Safety Information Which Form 4 to Use?
CareSearch: What is the Research Data Management System? This event is part of the Quality Use of CareSearch Project.
Advance and the Electronic Packet Advance and the Electronic Packet April 5,
Clinovo 1208 E. Arques Avenue, Suite 114 Sunnyvale, CA Thursday, June 23 rd 2011 Medidata Rave®
Frequency and type of adverse events associated with treating women with trauma in community substance abuse treatment programs T. KIlleen 1, C. Brown.
Andrew Thornton, Chairman, RAH HREC
Adverse Event Reporting.
RESCUE 4701 Adverse Event Reporting October 16, 2010 Maria Oh, Director Protocol Development & Regulatory Compliance.
EMORY INSTITUTIONAL REVIEW BOARD VERSION Unanticipated Problems, Protocol Deviations and Non-Compliance.
Monitoring the Progress of Trials and the Safety of Participants Don Workman, PhD Victor Santana, MD St. Jude Children’s Research Hospital.
RESCUE: ACRIN 4701 Protocol Development & Regulatory Compliance (PDRC) Josephine Schloesser, ACRIN Monitor Chris Steward, ACRIN QC Auditor.
MODULE B: Case Report Forms Jane Fendl & Denise Thwing April 7, Version: Final 07-Apr-2010.
The Stroke Hyperglycemia Insulin Network Effort (SHINE) Trial Brief Protocol Training NIH-NINDS U01 NS NETT CCC U01 NS NETT SDMC U01 NS
Mass BioTech Council DMC Presentation Statistical Considerations Philip Lavin, Ph.D. October 30, 2007.
SAE data entry: Clinical versus Pharmacovigilance standards Daniel Becker Solvay Pharmaceuticals Hannover, Germany T:
EAE Training EAE Reporting and Assessment Overview DAIDS Regional Training Event, Regulatory Compliance Center Kampala, Uganda, September 2009 DAIDS Regional.
Using EDC-Rave to Conduct Clinical Trials at Genentech Susanne Prokscha Principal CDM PTM Process Analyst February 2012.
I4ma Server Overview. High Level Architecture Internet Mobile Device Web Browser I4ma Server SMS SMS Service.
Clinical Trials and Research A Guide for Community Advisory Board Members Participant Manual.
CTRP User Call May 7, 2014 Gene Kraus CTRP Program Director.
The NCI Central IRB Initiative Jacquelyn L. Goldberg, J.D. VA IRB Chair Training April 8, 2004.
Navigating IRBs as a Suicide Researcher Peter M. Gutierrez, Ph.D. VISN 19 MIRECC American Association of Suicidology Annual Conference, April 19, 2012.
Conducting Research at Lincoln IRB/HRPP Policies, Procedures & Good Clinical Practices B Kanna MD, MPH, FACP Associate Program Director of Internal Medicine.
Sponsor Visits and Monitoring
ACRIN CV Committee ACRIN PDRC ACRIN PA 4008 Protocol and Regulatory Requirements Patricia Atkinson, Quality Control Monitor.
VA Central IRB K. Lynn Cates, MD Assistant Chief Research & Development Officer Office of Research & Development Department of Veterans Affairs September.
Speaking Clinical Trials Marianne Kearney Director of Research Operations Neurological Clinical Research Institute Massachusetts General Hospital.
Medidata Rave Start-Up Information
The NINDS Common Data Elements Project February 20, 2014 Wendy R. Galpern, MD, PhD NINDS / NIH American Society for Experimental NeuroTherapeutics | 16.
Responsibilities of Sponsor, Investigator and Monitor
Rare Diseases Clinical Research Network Data Management and Coordinating Center (RDCRN DMCC) Rosalie Holland LDN Investigator Meeting at WORLDSymposium.
1 SAE Centralized Report and Review Process April 2012.
Sponsor Visits and Monitoring Barbara Gallagher, RN Clinical Research Nurse Jefferson Clinical Research Institute.
Design of Case Report Forms
A New Algorithm for Unequal Allocation Randomization
Rachel Neubrander, PhD Division of Cardiovascular Devices
Keystone Heart Reflect Neurology
Responsibilities of Sponsor, Investigator and Monitor
HOW TO ENTER EARLY WITHDRAWAL DATA
Reportable Events Emory IRB 9/11/2014.
Clinicaltrials.gov Update
Safety Reporting Nichol McBee, MPH, CCRP.
Remote Monitoring of Adverse Events
Remote Monitoring of Adverse Events
ARCADIA Coordinator Webinar
Valerie Durkalski Medical University of South Carolina
Carolina Mendoza-Puccini, MD
Data Management in Support of A Clinical Event Committee (CEC)
Model Enhanced Classification of Serious Adverse Events
Region 8 Meeting Harvey Solomon, MD
11 iii. Define management and supervision roles and responsibilities
Adverse Event Reporting _____________________________
Presentation transcript:

Architecture Design of Generic Outcome Adjudication in CTMS Wenle Zhao, PhD Medical University of South Carolina, Charleston, SC, 29425, USA Society for Clinical Trials 36th Annual Meeting Arlington, VA, USA - May 17-20, 2015

Contents 1.The Motivation 2.The Challenges 3.The Generic Database Model 4.The Automated Coordination 5.Summary

1.The Motivation 2.The Challenges 3.The Generic Database Model 4.The Automated Coordination 5.Summary

Patients Randomization Treatment ATreatment B Outcome AOutcome B Analysis Accurate Outcome ( Endpoint) Assessment is Important The validity of the trial results relies on the accuracy of outcome assessment.

Outcome Safety OutcomeEfficacy Outcome AE is Serious?Quality of Life Modified Ranking Scale NIH Stroke Scale Hamilton Rating Scale for Depression Hamilton Rating Scale for Anxiety Most Outcome Assessments are Subjective AE is Expected? AE is Related to Study Treatment? Glasgow Outcome Scale Extended The Problem: Uneven expertise and potential bias The Solution: Independent central adjudication

1.The Motivation 2.The Challenges 3.The Generic Database Model 4.The Automated Coordination 5.Summary

Example 1: A Simple SAE Adjudication SAE CRF Submitted Is serious?Is expected?Is related? Done CRF Completed? May be not. How to notify the adjudicator? Auto . When it is expected? No schedule. Need more information? May be yes. CRF Updated after submission? Could happen.

Four challenges for coordinating outcome adjudication  Adjudication procedures vary among projects No fixed model for every procedure.  Timing of outcome event unpredictable No schedule.  Narrow time window for completion of adjudication “Time is of the essence.”  Data changing after adjudication procedure started The target is moving.

1.The Motivation 2.The Challenges 3.The Generic Database Model 4.The Automated Coordination 5.Summary

The Generic DB Structure for Adjudication Procedures 1 ∞ ∞ 1 ∞ ∞ 1 ∞ 1 Adjudication Procedure ID Form ID Procedure Name Adjudication Step ID Procedure ID Adjudication Step Name Enable-logic condition Disable-logic condition Question 1 Answer 1 Code Group ID …… Question 5 Answer 5 Code Group ID Edit User Group ID View User Group ID Adjudication Result ID Adjudication Step ID Record ID Freeze Record ID Answer 1 …… Answer 5 General Comments Locked Data (CRF) Form ID Form Name Table Name Form Table ID Subject ID Visit ID Q01 Q02 …… Updated By Updated On Form Freeze Table Freeze Record ID Subject ID Visit ID Q01 Q02 …… Updated By Updated On ID The Model Allow multiple steps. Allow multiple updates. Limit ≤ 5 close-ended Qs.

Two Tables are included in the Database Template

One table specifies definitions of each adjudication step. The other table stores adjudication results.

A freeze table is created for each data form table with adjudication

Adjudication Step Enable logicDisable logic Question 1 (Q1) Question 2 (Q2) Question 3 (Q3) Step 1 PM Review (S1) {New SAE CRF submission} {S2 submitted after S1} OR {S3 submitted after S1} CRF properly completed? 0 = No 1 = Yes Requires MSM review? 0 = No 1 = Yes Step 2 MSM Adjudication (S2) {S1Q1=1} AND {S1Q2=1} AND {no S2 submitted after S1} AND {no S3 submitted after S1} {S2 submitted after S1} OR {S3 submitted after S2} Serious? 0 = No 1 = Yes Unexpected? 0 = No 1 = Yes Related to study drug? 1 = Unrelated 2 = Unlikely 3 = Possible 4 = Probably 5 = Definitely Step 3 PM Review (S3) {S2 submitted} AND {no S3 submitted after S2} {S3 submitted after S1} MedWatch Form needed? 0 = No 1 = Yes Example 1: Definition of Three-step SAE Adjudication

Adjudication StepEnable logicDisable logic Question 1 (Q1) Question 2 (Q2) Step 1 Project Manager (PM) Review {New SAE CRF submission}{S2 submitted after S1} CRF properly completed? 0 = No 1 = Yes Requires CEC review? 0 = No 1 = Yes Step 2 Clinical Event Coordinator (CEC) Review {S1Q1=1} AND {S1Q2=1} AND {no S2 submitted after S1} {S1 submitted after S2} OR {S3 submitted after S2} OR {S4 submitted after S2} OR Even packet complete? 0 = No 1 = Yes Event type? 1 = Neurological 2 = Cardiac 3 = Systemic Step 3 Adjudicator 1 Review (S2Q1=1) AND {no S5 submitted after S3} {S1 submitted after S3} OR {S5 submitted after S3} Outcome category=? 1 = ischemic stroke 2 = symptomatic hemorrhagic transformation of an ischemic stroke 13 = transient ischemic attack Death type =? 1 = ischemic 2 = hemorrhagic vascular 3 = nonvascular Step 4 Adjudicator 2 (ADJ2) Review (S2Q1=1) AND {no S5 submitted after S4} {S1 submitted after S4} OR {S5 submitted after S4} Step 5 Adjudicator 3 (ADJ3) Review {S3 submitted after S1} AND {S4 submitted after S1} AND {S3Q1≠S4Q1 or S3Q2≠S4Q2} AND {no S6 submitted after S5} AND {S1 submitted after S5} OR {S6 submitted after S5} Step 6 Adjudication Committee Chair (ACC) Review {S5 submitted after S1} AND {S5Q1≠S3Q1 or S5Q2≠S3Q2} AND {S5Q1≠S4Q1 or S5Q2≠S4Q2} AND {no S1 submitted after S6} AND {S6 submitted after S1} Example 2: Definition of Six-step SAE Adjudication

The Generic Table for Adjudication Results

1.The Motivation 2.The Challenges 3.The Generic Database Model 4.The Automated Coordination 5.Summary

Site submits a Case Report Form Form has adjudication procedure defined? System evaluates enable logics for each adjudication steps Enable logic = true & disable logic = false? System sends to [Edit] user group members User views a Case Report Form User has adjudication step [Edit] permission & Enable logic = true & disable logic = false? System displays [Adjudication Edit] button for the user User adds/edits adjudication result and submits adjudication record The last freeze record is the same as the current CRF record? System creates new freeze record, links it to the adjudication record. Y Y Y N Y N N N Automated Coordination of Adjudication Activities

Site submits SAE CRF S1Q1 = Yes? Step S3 = PM Review S3Q1: MedWatch Form required? System composes MedWatch Form draft N Y Y N Step S1 = PM Reviews S1Q1: CRF properly completed? S1Q2: Requires MSM adjudication? Auto #1 to PM Auto #3 to MSM Auto #2 to Site S1Q2 = Yes? Step S2 = MSM Adjudication S2Q1: Serious? S2Q2: Unexpected? S2Q3: Related to study treatment? Site adds/edits SAE CRF Auto #4 to PM S2Q1 = Yes & S2Q2 = Yes & S2Q3 = Possible/ Probably / Definitely? S3Q1 = Yes? Auto #6 to Site Site edits MedWatch PM Closes the Adjudication Procedure Auto #7 to PM PM finalizes MedWatch and submits to FDA Auto #8 to All Sites N Y Auto #5 to PM Y N Example 1: Three-step SAE Adjudication Procedure

Site submits SAE CRF S1Q1 = Yes? Step S3 = ADJ1 Review S3Q1: Outcome category? S3Q2: Death type? Y N Step S1 = PM Reviews S1Q1: CRF properly completed? S1Q2: Requires CEC review? Auto #1 to PM Auto #3 to CEC Auto #2 to Site S1Q2 = Yes? Step S2 = CEC Adjudication S2Q1: Event packet complete? S2Q2: Event type? Site adds/edits SAE CRF and upload the event packet Auto #7 to ADJ3 Auto #9 to PM PM Closes this Adjudication Procedure N Y Auto #5 to ADJ1 Y Step S5 = ADJ3 Review S5Q1: Outcome category? S5Q2: Death type? Step S4 = ADJ2 Review S4Q1: Outcome category? S4Q2: Death type? S3 = S4? Auto #6 to ADJ2 N System determines adjudicators 1, 2, and 3 based on S2Q2 and the Random number R. Auto #4 to Site Y S2Q1 = Yes? N Auto #8 to ACC Y Step S6 = Chair Review S6Q1: Outcome category? S6Q2: Death type? S3= S5 or S4 = S5? N Example 2: Six-step Outcome Adjudication Procedure

In this case, the Clinical Event Coordinator (CEC) completed the adjudication within few hours after the Study Manager (SM) ‘s completeness review passed.

In this case, the procedure has not been completed yet after two months, due to CRF data change.

1.The Motivation 2.The Challenges 3.The Generic Database Model 4.The Automated Coordination 5.Summary

Adjudication Procedure From stepTo step Event count 1st quartile (25%) 2nd quartile (50%) 3rd quartile (75 %) hrs Three-step SAE adjudication CRF submitPM review PM reviewMSM review MSM reviewPM close Six-step outcome event adjudication CRF submitPM review PM reviewCEC review CEC reviewADJ1/2 review ADJ1/2 reviewADJ3 review ADJ3 reviewACC review PM: project manager MSM: medical safety monitor CEC: clinical event coordinator ADJ1/2: adjudicators 1 and 2 ADJ3: adjudicator 3 ACC: adjudication committee chair Our Experiences

The Strategy to Success  Allows multiple adjudication procedures per CRF.  Allows multiple steps for each adjudication procedure.  Allows different questions be asked for each adjudication step.  Only close-ended questions are allowed.  No more than 5 questions are allowed.  Using automated s to help adjudication coordination.  Allows multiple CRF submissions after adjudication started.

Acknowledgement This research is partly supported by following NIH/NINDS grants: U01NS (NETT Palesch, Y. & Durkalski, V.) U01NS062778(ProTECT, Palesch Y.) U01NS062835(POINT, Palesch, Y.) U01NS087748(StrokeNet, Palesch, Y. & Zhao, W.)  The followings are contributed to the design, development, validation and user feedback collection to this work: Keith Pauls(DCU senior programmer) Jaemyung Kim(DCU senior programmer) Catherine Dillon(DCU senior data manager) The Clinical Coordination Center of the NINDS NETT at University of Michigan  Thousands investigators in hundreds institutions and thousands patients participating our clinical trials.

Thank You! Contact me at: