Request for OMB Approval for an
Emergency Information Collection Request
Submitted: May 18, 2015
Program Official/Project Officer
Barbara Knust, DVM, MPH, DACVPM
CDR, US Public Health Service
Viral Special Pathogens Branch
US Centers for Disease Control
404-639-1104 phone
404-639-1118 fax
404-218-9626 mobile
Part B — Collections of Information Employing Statistical Methods 3
1. Respondent Universe and Sampling Methods 3
2. Procedures for the Collection of Information 5
3. Methods to Maximize Response Rates and Deal with Nonresponse 9
4. Test of Procedures or Methods to be Undertaken 9
5. Individuals Consulted on Statistical Aspects and Individuals Collecting and/or Analyzing Data 10
This research study will enroll individuals with documented previous Ebola virus (EBOV) infection from four study sites in three high EVD burden districts in Sierra Leone (Western, Bombali, and Port Loko). Ebola virus disease (EVD) survivors at different points of convalescence, ranging from the time of discharge from an Ebola Treatment Unit (ETU) up to 30 weeks of convalescence, will be targeted for enrollment.
Eligible participants are adults (18 years of age or older) and must demonstrate an EVD discharge certificate and a national identification card in order to be recruited. In order to ensure survivor status and eligibility for the study, results may be cross-checked against the national laboratory database. Eligibility for each component of the study is as follows:
Pilot — Adult male (18 years or above) survivors will be enrolled if eligible, with assistance of the survivors association in Freetown and the collaborating hospital and clinic.
Module A — All adult men or women (18 years or above), discharged from an ETU or selected from survivor registries with a certificate of recovery, are eligible.
Module B — Lactating women (18 years or above), discharged from an ETU or selected from survivor registries with a certificate of recovery are eligible.
As this project will be conducted in the midst of an ongoing public health response, sample sizes may be adjusted by the Sierra Leone Ministry of Health and Sanitation (MoHS) and the Ministry of Social Welfare, Gender, and Children’s Affairs (MSWGCA) in accordance with national and local capacity and in a manner such that they will not interfere with response efforts. The number of participants will depend largely upon the number of EVD survivors from the selected clinic sites who can be located and agree to provide body fluid specimens.
Sample sizes for each component of the study are as follows:
Pilot — A maximum of 100 patients will be included with a target of 40% between 2 and 3 months convalescence period and 60% with over 3 months convalescence period.
Module A — There will be two relevant enrollment targets:
New survivors sample: recruitment of up to 16 (max) patients per week (if excess available this may be expandable dependent on capacity to investigate further numbers without detriment to local care provision, if not then recruitment shall be of equal gender distribution if possible) during a recruitment period expected to last one month
Established survivor sample:
A sample of 50 patients (25 male + 25 female) will be enrolled, these are all at less than or equal to 4 weeks post discharge
300 patients (150 male + 150 female) will be recruited at greater than 4 weeks post discharge, but less than 30 weeks. No more than 10 patients of a single gender shall be recruited into a single week
Module B — Participants meeting eligibility criteria may be rare and it may be that relatively few mothers will have those characteristics and be able to provide the requested milk and sweat specimens. A target of 100 lactating women will be enrolled in Module B.
If the number of patients discharged from ETUs per week is no longer sufficient to meet study sample sizes (i.e., by the time Modules A and B are implemented), it is anticipated that there will be adequate numbers of potential participants in survivor registries to meet the study sample sizes.
For the primary outcome of live virus isolated in tissue culture, even one positive result is of interest; as such a finding would be expected to have important implications for guidance to future caregivers, patients, and their families. Similarly, we would not want to conclude that there is no probability of persistent live EBOV virus in the fluids we test if, in reality (within the larger population), there is. Therefore, the primary power calculation of interest is the degree of confidence we can have in a null (no positives) result from our tissue culture testing. In other words, we need to know the upper confidence limit for a calculated proportion of 0% in our study.
There are several ways to calculate an upper bound for a 95% confidence interval for a 0% finding. The rule of thumb for the upper bound is 3/N, where N is the number of specimens tested. This method is accurate when the sample is sufficiently large. Calculating the upper bound precisely requires use of the binomial distribution. The table below lists the upper bounds for a 1-sided 95% confidence interval estimated using Stata SE V12.1:
Numerator |
0 |
0 |
0 |
0 |
Denominator |
50 |
100 |
200 |
300 |
|
|
|
|
|
Upper bound |
7.1% |
3.6% |
1.8% |
1.2% |
Lower bound |
0% |
0% |
0% |
0% |
Survivor associations in each of the districts will be involved with the study implementation. A small group of survivors will be formed to serve as key informants for sensitization of the community and recruitment for the study.
In collaboration with the survivors association and the MSWGCA, a list of established EVD survivors will be selected in accordance with sample size criteria. These groups of established survivors will be invited to a meeting in their district where they will be informed about the study process and benefits by MSWGCA staff and/or survivor key informants. The interested participants will be asked to review and sign the informed consent and an appointment will be scheduled for the first study visit. In addition print and radio advertisements may be used to recruit for the study.
Pilot
The recruitment of survivors for the pilot will be done on a voluntary basis with the help of the association of survivors in Freetown and before the samples for Module A and B are selected. A collaboration with the national survivors’ association has already been started, and the organization has been part of the formative work. The association foresees no challenges in recruiting participants for the pilot study.
Module A
Recruitment from the ETUs |
All adult patients newly discharged from an ETU during the recruitment period will be asked to participate in the study |
Recruitment from survivor registry |
Survivors will be contacted according to their duration of convalescence and their place of residence. |
Recruitment from other sources |
If the number of patients is not enough, an open cohort process where participants will be recruited by using local ETU records, survivor networks and services; community outreach, including radio solicitations, may also be considered. |
|
|
Module
B
Recruitment from the ETUs |
All lactating female survivors newly discharged from an ETU during the recruitment period may be asked to participate in the study |
Recruitment from survivor registry |
As no information on lactation status is available, if a female survivor in Module A is lactating, she will be proposed entry into Module B. |
Recruitment from other sources |
If the number of patients is not enough, an open cohort process where lactating female survivors will be recruited by using local treatment center records, survivor networks and services; community outreach, including radio solicitations, may also be considered. |
The Sierra Leone MoHS will ensure coordination of project activities with routine MoHS response activities. Data from routine MoHS response activities (case investigation and contact tracing) will be shared for project purposes as needed. The Sierra Leone MoHS will advise in hiring local clinical and data entry staff. Clinical staff will interact with participants; clinical and data entry staff will have access to individually identifiable data. CDC and WHO will provide technical assistance in all project aspects and will supervise clinical staff and lead data analysis. As supervisory staff, CDC and WHO field staff will interact with participants and have access to individually identifiable data.
The MoHS identified four study sites in three high EVD burden districts (Western, Bombali, and Port Loko) for the study:
M34 hospital, Freetown (pilot site location)
PTS1 (Police Training Station) Hospital
Makeni District Hospital
Port Loko Government Hospital
For the pilot study and both modules, the study site(s) will be the setting for all initial and follow-up visits of survivor participants. These study sites will be the location for interviews, specimen collection, and counselling regarding test results. Study participants can be referred to HIV and survivor services within the hospitals where the study sites are located.
For the study:
Eligible study participants must demonstrate an EVD discharge certificate and a national identification card in order to be recruited. To ensure survivor status and eligibility for the study, collaborators may cross-check laboratory information as available. This information will be recorded in the Intake Form (Attachment 1) and a unique ID will be assigned.
Entry will then begin with the informed Consent Form (Attachment 2 or Attachment 3; for pilot study/Module A or Module B, respectively).
A Participant Study ID Card (Attachment 4) will be issued to the participant, and a photo will be taken for verification of identity at subsequent study visits.
The participant will then complete a Survivor Questionnaire (Attachment 5) and initial specimen collection.
Specimen(s) will be tested for EBOV RNA by RT-PCR in Sierra Leone at the CDC laboratory facility in Bo; any specimen positive for EBOV by RT-PCR will be frozen and shipped to CDC for culture/virus isolation in a BSL-4 laboratory facility in Atlanta, GA.
Participants with a RT-PCR positive result in any of the initial specimens will be invited to complete a Survivor Follow-up Questionnaire (Attachment 6) at every subsequent study visit and to provide prospective specimens (i.e., repeat specimen collection) of each RT-PCR positive body fluid according to the following schedule:
Semen collection every 2 weeks for the first three visits and then monthly until the RT-PCR is negative (pilot).
Specimen (i.e., semen or vaginal secretions, rectal swabs, sweat, urine, saliva, tears) collection every 2 weeks for the first three visits and then monthly until the RT-PCR is negative (Module A)
Specimen (i.e., sweat and breast milk) collection every 3 days until the RT-PCR is negative (Module B)
All laboratory results will be entered into a Laboratory Results Form (Attachment 7) marked with the participant’s study ID and kept in confidential storage for entering of follow-up results.
At follow up visits, laboratory results will be shared with the participant, and transmission prevention and potentially other counselling messages will be provided via a Counselling Script (Attachment 8).
Confirmatory virus culture results will be reported back to participants when available.
Once a participant has had two consecutive negative test results for all body fluid specimens collected in this study, there will be no further follow-up.
At the study sites
All biological specimens will be kept cold and will be transported from the study sites to the CDC Bo laboratory daily (three times weekly during the pilot study).
All sampling and handling of specimens collected for transportation should follow procedures for labeling, packaging, transporting, and storing bio-hazardous material.
At CDC Bo laboratory:
RT-PCR will be performed on all specimens for two viral targets, viral matrix protein 40 (VP40) and nucleoprotein (NP), as well as an internal human control, human beta-2-microglobulin (B2M), according to standard guidelines.
If the internal human control is negative for a given specimen, this would be viewed as an inadequate sample and a new specimen would be requested.
Specimens will be stored at -70C and those that are RT-PCR positive at the CDC Bo laboratory will be shipped to the CDC-Atlanta BSL-4 laboratory for virus isolation testing, following appropriate protocols for transporting Category I biohazards.
CDC Atlanta BSL-4 laboratories:
In order to determine if a given body fluid specimen has live virus and is potentially infectious, virus culture will be performed. This can only be safely performed in Biosafety Level (BSL)-4 laboratory conditions, which are not available in Sierra Leone. Therefore specimens which have detectable EBOV RNA by RT-PCR will be transported frozen with adequate safe packaging and cold chain to Atlanta, GA, USA for virus isolation.
Testing for live virus will be performed at the CDC BSL-4 laboratory in Atlanta, GA, USA, ideally within 6 months of specimen receipt. Standard EBOV virus isolation protocols for diagnostic specimens will be followed.
If specimen type and volume permit, the viral titer (TCID50/mL) for the specimen will be determined. This will inform the amount of infectious virus in a specimen, unlike virus isolation which will tell you a binary (i.e., yes or no), to infectious EBOV virus in the specimen.
Residual body fluid specimens will be destroyed. Viral isolates, if any, may be preserved at CDC for further study in collaboration with MoHS and WHO (in accordance with the research collaboration agreement). Body fluid isolates will be kept in liquid Nitrogen frozen storage (-165C) in a secure location at CDC’s BSL-4 laboratory. Virus isolates can be shared to requesting parties assuming that the requesters can comply with the necessary biosafety requirements (BioSafety Level-4, Select Agent compliance). Further study of virus isolates may include genetic analysis and comparison with other virus strains.
All MoHS-owned data related to a study participant will be assigned the participant’s unique study ID. No patient-identifying information (i.e., names) will leave Sierra Leone.
Interview data will be organized in databases stored on secure local servers within the Ministry of Health in Sierra Leone and WHO and will be backed-up regularly. Collected data will be directly recorded on computers or tablets to minimize data recording and entry errors and minimize delays in data availability. If paper forms must be used, interview responses will be entered into the database either daily or as a group at the close of data collection; and 10% of entered forms will be re-checked to identify any problems with data entry accuracy that must be addressed.
Electronic equipment and files will be kept password-protected.
Paper forms and electronic devices will be kept locked when not in use.
All individual data identifying direct patient identifiers will be removed from the dataset before analysis and replaced with a unique participant code that can be linked back to individuals via a master key at a centralized secure server and database.
Individual records and the key linking the participant code number will be kept secure, accessible only to the local study team under the supervision of the study PI and MoHS in collaboration with WHO and CDC.
Paper interview forms, if used, will be destroyed within one year after all data are entered and verified.
Laboratory results will be batch processed and complete PCR results for all specimen types will be reported back within 1 week of specimen receipt to each site coordinator. A positive RT-PCR result on any specimen should be entered in the secured data base and reported within 8 hours to the study PI and WHO and CDC local coordinators as well as the site coordinator where the specimen was collected. Laboratory staff will identify specimens only by the labelled study ID, and will not have access to any personally identifying information.
Site coordinators will provide laboratory results only in person and only to participants who (1) return for a follow-up study visit; and (2) present their study ID card or confirm their identity and study ID number; and (3) request to receive their own results. Individual results will not be shared with anyone other than the study participant. Results will be presented according to the counselling script in Attachment 8.
Viral isolation results from CDC Atlanta will be reported promptly to the study PI and entered in the secured data base as they arrive. These confirmatory results will not be available within a clinically relevant time frame (6 months) although positive results will be reported to participants.
As previously noted, survivor associations in each of the districts will be involved with the study implementation. A small group of survivors will be formed to serve as key informants for sensitization of the community and recruitment for the study. Study participation is voluntary, and study leads will make every effort to maximize the rate of response. Additionally, support will be offered to every participant at every visit including: specific EBOV transmission prevention counselling and provision of condoms distributed by trained counsellors; voluntary human immunodeficiency virus (HIV) testing and counselling will be offered to all participants, and HIV-positive study participants will be referred for HIV counselling and treatment services; participants in need of specific health services will be referred to the appropriate clinic/hospital for care and management. When pertinent, counselling on potential EBOV transmission via breastfeeding will be given by trained counsellors and alternative feeding will be provided. The counselling script (Attachment 8) addresses many anticipated study participant questions. Finally, several survivors’ support groups are actively working to provide counselling and support of various qualities to EVD survivors in Sierra Leone, in collaboration with UNICEF and the national survivors’ association, which study collaborators anticipate will mitigate community concerns.
Main challenges to the success of the project include willingness of participants to provide biological specimens from sensitive locations, and to share intimate information on sexual behavior. Proposed solutions are to ensure trained interviewers and medical staff of appropriate genders and cultural backgrounds, who are used to discussing sexual behavior, and to take bio-samples of sensitive character. Also to secure an environment where the interviewee will be secure the procedures and information is kept confidential. The ability to provide quick turnaround of specimen processing and analysis for timely report back to participants, especially in the breast milk Module B will also be a challenge.
Every effort will be given to maintaining communication with enrolled participants. Contact information of the participant will be collected and contact information for local study staff will be provided at enrollment.
Using WHO funds only, the study team previously held a focus group with 15 male EVD survivors at the Military 34 hospital grounds; CDC personnel observed, but did not conduct, this focus group. The study team provided an overview of the study and explained the rationale, followed by a review of the informed consent and questionnaire with the group. The group provided feedback on their comprehension of the informed consent, the acceptability of the subject matter, and questionnaire content. Revisions were made to the informed consent and questionnaire based on this feedback. The group did not find the informed consent or questionnaire process burdensome.
The pilot study is intended to
Inform the process and implementation of the overall study (i.e., Modules A and B)
Provide rapid results on the prevalence of EBOV by RT-PCR in semen of survivors
Assess the prevalence of live Ebola RNA detected by culture/viral isolation from RT-PCR positive semen
Only minor study changes are expected, if any. As a result, a combined approval for the pilot and the subsequent modules is preferred. Any changes to the procedures or methods to be used will be communicated to IRB and OMB as quickly as possible before data collection for Modules A and B begins.
Role |
Name |
Telephone Number |
|
Statistical consultation |
Tim Flietstra |
404.639.1137 |
hng8@cdc.gov |
Data collection and/or analysis |
MoHS |
|
|
Gibrilla Fadlu Deen |
NA* |
gibrilladeen1960@yahoo.com |
|
Amara Jambai |
NA |
amarajambai@yahoo.com |
|
Alie Wurie |
NA |
wuriealieh@yahoo.com |
|
Tina Davies |
NA |
tngebeh@hotmail.com |
|
Foday Sahr |
NA |
fsahr@yahoo.com |
|
Foday Sesay |
NA |
NA |
|
WHO |
|
|
|
Nathalie Broutet |
NA |
broutetn@who.int |
|
Anna Thorson |
NA |
thorson.a@gmail.com |
|
Teodora Wi |
NA |
wit@who.int |
|
Kara Durski |
NA |
durskik@who.int |
|
Jaclyn Marrinan |
NA |
marrinanj@who.int |
|
Lee Sharkey |
NA |
leedsharkey@gmail.com |
|
Theo Grace |
NA |
gracet@who.int |
|
Faiqa Ebrahim |
NA |
ebrahimf@un.org |
|
CDC |
|
|
|
Barbara Knust |
404.639.1104 |
bkk0@cdc.gov |
|
Oliver Morgan |
404.553.7318 |
ggv7@cdc.gov |
|
Christine Ross |
404.528.0490 |
wiz6@cdc.gov |
|
Dianna Ng |
404.639.0069 |
ydd9@cdc.gov |
|
Sarah Bennett |
404.639.2274 |
iyk3@cdc.gov |
|
Elizabeth Ervin |
404.639.0038 |
wkc8@cdc.gov |
|
Kyle Bernstein |
404.960.9183 |
kio8@cdc.gov |
|
Elissa Meites |
404.704.2427 |
dri9@cdc.gov |
|
Administrative Support |
Rachel Kaufman |
404.498.2347 |
rbk8@cdc.gov |
Michael Fox |
404.498.3806 |
Imv9@cdc.gov |
|
Neil Rainford |
770.488.1122 |
ner0@cdc.gov |
|
Tara Anderson |
404.498.6314 |
tqc3@cdc.gov |
*Not Available (NA)
APPENDIX A. Authorizing Legislation
APPENDIX B. Human Subjects Review and Approvals
APPENDIX C. Sierra Leone News 2015 Minimum Wage
ATTACHMENT 1. Intake Form
ATTACHMENT 2. Consent Form – Pilot and Module A
ATTACHMENT 3. Consent Form – Module B
ATTACHMENT 4. Participant Study ID Card
ATTACHMENT 5. Survivor Questionnaire
ATTACHMENT 6. Survivor Follow-up Questionnaire
ATTACHMENT 7. Laboratory Results Form
ATTACHMENT 8. Counselling Script
| File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
| File Title | O2C2-Supporting-Statement-B-Template-CDCID-NICKNAME-SSB |
| Author | gel2 |
| File Modified | 0000-00-00 |
| File Created | 2021-01-25 |