Skip to Content
Interactive Textbook on Clinical Symptom Research Logo


Home Button

Clinical Trials in TMD Sections
Author Bio
Introduction
The Biopsychosocial Model
Designing Multicenter RCTs
Players in an RCT
Randomization
Trial Design Quality
TMD Case Definition
Endpoints and Outcome Measures
Blinding & Masking
Study Sample Size
Number and Nature of Interventions
Study Length and Follow up
Intent-to-treat Analyses and Sample Size
Compliance
Multicenter RCTs
Currently selected section: Implementing RCTs: Practical Issues
Analysis of TMD Trials
Conclusions
Acknowledgments
Appendix A
Appendix B

 

Chapter 22: Clinical Trials in Temporomandibular: Multicenter RCTs
        

Communication

As has already been alluded to, communication among all study personnel is essential in RCTs. Regular electronic mail lists, in-person meetings, and routine data monitoring reports are all required to keep the trial on schedule.

Multicenter trials commonly have web sites that have both public and private sections; private sections require passwords to keep information available only to those people that need access.

Steering committees should meet on a regular basis, even weekly until the trial has begun and input from study personnel at all levels--investigators, data managers, administrative staff-- should be periodically obtained.

 

 

 

 

 


Page 60 of 81
      Previous Page