What to do if your proposal is accceptedFinal Acceptance = provisional acceptance + IRB approval + a successful trial run.What is provisional acceptance? Provisional acceptance is necessary but not sufficient for data collection on to begin. Two additional steps must be taken: the proposal must obtain human subjects approval and it must have a successful trial run. Human Subjects Documentation Fax: (215) 746-2911 Attention: Diana Mutz We encourage investigators to obtain IRB approval as soon as possible. The longer a researcher waits to get such approval, the longer will be the delay in collecting their data. To ensure subjects' protection, IRB's often want to know what subjects are told when they are recruited and what questions are used to elicit their demographic information. The scripts used for such purposes in our Internet-based experiments can be found here. (Note: These scripts are viewable only by people who have completed a TESS User Profile.) To repeat, if a proposal is accepted for placement on a TESS data collection instrument and if the investigators cannot obtain IRB approval, then it is ineligible for inclusion on a TESS data collection instrument. What is a successful trial run? In some cases, the consultation and trial run activities reveal that the actual amount of resources required to conduct the proposed experiment is more than initially anticipated. For example, trial run may show that an experiment budget for two minutes of time actually requires five minutes. Since TESS is a shared instrument, the time limits are strict. The subcontractor and TESS PI's will work with the investigator to fit their experiment into the allocated space. In the event that this cannot be accomplished to the satisfaction of the investigator, there are two options. If we can provide the additional service without decreasing our service to other accepted proposals, then we will ask the investigator to pay the additional costs. If this is not acceptable, then we will ask the investigator to consider submitting a revised proposal to TESS or to consider data collection opportunities that do not involve TESS. As a general rule most problems of this kind can be avoided if investigators conduct trial runs of their own before sending a proposal. What happens after I get human subjects approval and have a successful trial run? When will I receive the data from my experiment? For how long will I have exclusive access to the data from my proposal? What are my obligations to TESS after I receive my data? Investigators must also agree to prepare a summary description of their results including frequency tables for control and treatment groups presented in a uniform tabular format (which TESS will supply) by the end of the nine-month period. We will post the report immediately on our website and circulate news of the findings via e-mail lists and press releases. To increase the speed at which new knowledge is made broadly available, we also require the investigators to notify us of any working papers or publications based on the experiments. We then provide links to such papers on ExperimentCentral.org. |
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