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University of Colorado Cancer Center

University of Colorado Cancer Center, A National Cancer Institute-designated Comprehensive Cancer Center
 

Overview of Study Sequence


A typical study process will start with a researcher contacting the SRSR, we ask that you provide us some background on your project that will help us assess your needs.

We will then follow up with you and agree on a scope of work. Following IRB approval of your script (if needed) the SRSR will program your survey instrument and begin alpha and beta testing.

Once the programmed script meets with your approval the interviewers will begin data collection.

During field work we can produce different reports to best fit your needs; we can produce reports weekly, monthly or at another specified interval.

Once data collection is finished, the SRSR will produce a final data report including raw data files for analysis.

 

Final Data Report - Example Table of Contents

 

1. PROJECT OVERVIEW 

  • This section provides a brief synopsis of the study design and scope of work.

2. PROGRAMMED INTERVIEW

  • The programmed interview used during the study is contained in this section, which details all questions and corresponding flow logic.

3. DATA DICTIONARY

  • The study specific data dictionary is contained in this section.

4. FINAL DISPOSITION CODES

  • Final disposition codes are contained in this section and detail response rates for the project.
    • A. Disposition Report, only by last disposition completed by the SRSR
    • B. Disposition Report, all dispositions with breakdown of number of attempts by the SRSR

5. LIST OF DATA SETS, WITH ELECTRONIC VERSIONS

  • This section contains a list of all electronic data sets and study reports included in the final data deliverable. An analytic file, prepared in either SAS or SPSS can also be provided.