Get the free COMBINE Trial DMS Users Guide - cscc unc
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This Users Guide provides detailed instructions for operating Version 1.7 of the COMBINE Trial Data Management System (DMS), covering data entry, utilities, report generation, and important system
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How to fill out combine trial dms users
How to fill out COMBINE Trial DMS Users Guide
01
Begin by gathering all necessary patient data and documentation.
02
Access the COMBINE Trial DMS interface and log in with your credentials.
03
Select the appropriate trial and participant profile to begin the entry process.
04
Fill out the demographic information accurately, ensuring that all fields are completed.
05
Input medical history and any relevant pre-screening notes for the participant.
06
Document all assessments and evaluations as per the guidelines provided in the manual.
07
Review the entered data for accuracy before submission.
08
Submit the information and confirm that it has been correctly recorded in the system.
09
Follow up by checking for any alerts or notifications regarding the data submission.
Who needs COMBINE Trial DMS Users Guide?
01
Researchers conducting the COMBINE Trial.
02
Clinical staff involved in data entry and management.
03
Regulatory personnel who require detailed trial documentation.
04
Data managers monitoring patient information and trial progress.
05
Anyone involved in the oversight or compliance of the trial.
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People Also Ask about
What is combine study?
The COMBINE study evaluated treatment response to novel medication and psychosocial treatment combinations for 1,383 alcohol-dependent, treatment-seeking patients from 11 US sites. What follows is a brief summary of the design and results of the COMBINE study.
What is the focus of the combine approach to treating alcohol use disorders?
Although the primary aims of COMBINE were to test the incremental improvement of different treatment combinations on alcohol consumption, a secondary goal of the study was to explore client evaluations of various treatment combinations.
What is compain study?
The COMBINE Study is the largest pharmacotherapy trial conducted for Alcohol Use Disorder in the United States. This clinical trial evaluated the efficacy of naltrexone and acamprosate, both alone and in combination, in the context of medical management with and without Combined Behavioral Intervention (CBI).
What is the combine study?
The COMBINE study evaluated treatment response to novel medication and psychosocial treatment combinations for 1,383 alcohol-dependent, treatment-seeking patients from 11 US sites. What follows is a brief summary of the design and results of the COMBINE study.
What is combined behavioral intervention?
Combined Behavioral Intervention. Manual: A Clinical Research Guide for Therapists Treating People With Alcohol Abuse and. Dependence.
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What is COMBINE Trial DMS Users Guide?
The COMBINE Trial DMS Users Guide is a document that provides detailed instructions and guidelines for users involved in the COMBINE Trial Data Management System, ensuring proper data collection and management practices.
Who is required to file COMBINE Trial DMS Users Guide?
All researchers, coordinators, and staff involved in the COMBINE Trial who are responsible for data entry and management are required to follow and file the COMBINE Trial DMS Users Guide.
How to fill out COMBINE Trial DMS Users Guide?
To fill out the COMBINE Trial DMS Users Guide, users should follow the step-by-step instructions provided in the guide, ensuring that all required sections are completed accurately and all necessary information is included.
What is the purpose of COMBINE Trial DMS Users Guide?
The purpose of the COMBINE Trial DMS Users Guide is to standardize data management procedures, facilitate effective communication among team members, and ensure the integrity and quality of the trial data.
What information must be reported on COMBINE Trial DMS Users Guide?
The information that must be reported on the COMBINE Trial DMS Users Guide includes participant demographics, trial protocols, data collection activities, adverse events, and any other relevant data as specified in the guidelines.
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