NCHHSTP Generic Information Collection Request
OMB No. 0920-0840
Exp. 02/29/2016
Submitted: 12/16/2015
Program Official/Project Officer
Kendra Cuffe
Health Scientist
Centers for Disease Control and Prevention
1600 Clifton Rd NE Mailstop E-02
404 639 1847
Section B – Information Collection Procedures 3
1. Respondent Universe and Sampling Methods 3
2. Procedures for the Collection of Information 3
3. Methods to Maximize Response Rates Deal with Nonresponse 4
4. Test of Procedures or Methods to be Undertaken 4
5. Individuals Consulted on Statistical Aspects and Individuals Collecting and/or Analyzing Data 4
Eight US counties were included in the study sample based on a high county-level 2012 STD rates in at least three of the four following disease areas: gonorrhea, primary and secondary, syphilis, chlamydia, and HIV. Investigators will use convenience sampling methods in which an internet search of correctional facilities (i.e. jails, prisons) in the chosen areas will be performed. A letter will be emailed to each correctional facility’s Chief of Medical Operations explaining study purpose and methodology and requesting that a staff member that is involved with inmate health care be recommended for a key informant interview (see Attachment 5—Notification Email). A follow-up phone call will be made within 7 days to each of Chief of Medical Operations to provide the opportunity to address study questions or concerns, assure the protection of key informant identity, and address other confidentiality issues (see Attachment 6—Follow up Phone Script). The other purpose of the call is to potentially identify the key informant to be interviewed and then schedule the interview. Key informants may be asked to refer additional key informants and facilitate communication. Key informants may include physicians, prison guards who oversee STD patients, nursing staff, and/or STD counselors/testers.
At least one key informant interview will occur for each prison selected.
State |
County |
Number of Key informants to be interviewed |
CA |
LA |
1-3 |
IL |
Cook |
1-3 |
FL |
Miami-Dade |
1-3 |
GA |
Fulton |
1-3 |
NY |
Kings |
1-3 |
PA |
Philadelphia |
1-3 |
TX |
Dallas |
1-3 |
TX |
Harris |
1-3 |
Total |
8 |
8-24 |
Data for this study will be collected through key informant interviews. The interviewer, the Senior Project Director in the Public Health Management Corporation, will use a semi-structured interview guide as the data collection tool (see Attachment 3—Instrument: Key Informant Interview Guide). The guide will contain a series of open-ended questions and probes to illicit responses from key informants. Chief of Medical Operations in the jails and prisons in the sample will be sent an initial communication via email requesting that a health care provider be recommended for a key informant interview (see Attachment 5—Notification Email).
The primary notification email will explain:
The purpose and methodology of the overall study
Request that a staff member involved in inmate health care be recommended for the key informant interviews
That a follow-up phone call will be made within 7 business days
Interviews will be scheduled in advance during the follow-up phone call made to the facility Chief of Medical Operations.
The follow-up phone call (see Attachment 6- Follow up Phone Script) will explain:
That protection of key informant identity is assured
That participation is voluntary
The expected time to complete the assessment
Contact information for the investigation team
Although participation in the assessment is voluntary, the project lead will make every effort to maximize the rate of response. The key informant interview tool was designed with particular focus on open-ended questions to allow the respondent to provide a wealth of detail on topics of interest (i.e. STD screening, testing, and treatment protocols, etc…). The respondent will have the option to skip questions he does not feel comfortable asking. Respondents will be informed that they will have the right to end the interview at any time.
The estimate for burden hours is based on a pilot test of the information collection instrument by [1] of public health professionals. In the pilot test, the average time to complete the instrument including time for reviewing instructions, gathering needed information and completing the instrument, was approximately [70] minutes. Based on these results, the estimated time range for actual respondents to complete the instrument is [60] to [70] minutes. For the purposes of estimating burden hours, the upper limit of this range (i.e., [70] minutes) is used.
Archana Bodas LaPollo, Senior Project Director, Public Health Management Corporation, archana@phmc.org
Fellow TDB, Fellow, Public Health Management Corporation, TBD
Jami Leichliter, Supervisory Health Scientist, CDC, gzl3@cdc.gov
Harrell Chesson, Health Economist, hbc7@cdc.gov
Ryan Cramer, Public Health Advisor, uxj0@cdc.gov
Kendra Cuffe, Health Scientist, kkn2@cdc.gov
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