This PDF is the current document as it appeared on Public Inspection on 10/14/2016 at 08:45 am.
The Centers for Disease Control and Prevention (CDC) has submitted the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The notice for the proposed information collection is published to obtain comments from the public and affected agencies.
Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address any of the following: (a) Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; (b) Evaluate the accuracy of the agencies estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (c) Enhance the quality, utility, and clarity of the information to be collected; (d) Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses; and (e) Assess information collection costs.
To request additional information on the proposed project or to obtain a copy of the information collection plan and instruments, call (404) 639-7570 or send an email to firstname.lastname@example.org. Direct written comments and/or suggestions regarding the items contained in this notice to the Attention: CDC Desk Officer, Office of Management and Budget, Washington, DC 20503 or by fax to (202) 395-5806. Written comments should be received within 30 days of this notice.
Study to Explore Early Development (SEED) Phase 3—New—National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Autism spectrum disorders (ASD) are a group of neurodevelopmental disorders characterized by qualitative impairments in social interaction and communication and stereotyped behaviors and interests. Recent systematic population surveys and routine monitoring systems in the U.S. and other countries indicate the prevalence to be 1-2%. Apart from the identification of some rare genetic conditions that are commonly associated with autism, causal mechanisms for the disorder largely remain unknown.
The Children's Health Act of 2000 mandated CDC to establish autism surveillance and research programs to address the number, incidence, and causes of autism and related developmental disabilities. Under the provisions of this act, NCBDDD funded five Centers for Autism and Developmental Disabilities Research and Epidemiology (CADDRE) through program announcements in FY2001 and FY2002; CDC's NCBDDD served as the sixth CADDRE site.
For the first funding cycle (2001-2006), each CADDRE grantee had three core objectives: To develop a protocol for a multi-site collaborative epidemiologic study focused on autism (which was eventually named the Study to Explore Early Development [SEED]); to conduct surveillance of autism and other developmental disabilities; and to conduct site-specific investigator-initiated studies on autism. In FY 2006, through a second CADDRE funding cycle, five grantees were awarded. The CADDRE activities for the second funding cycle (2006-2011) were limited to implementation of the first phase of SEED (subsequently known as SEED 1). CDC served as the sixth CADDRE SEED 1 site during this period. A second phase of SEED (SEED 2) was funded under a third funding cycle (2011-2016). Five CADDRE grantees received the awards. Again, CDC served as the sixth SEED 2 site.
A third phase of SEED (SEED 3) was funded in July 2016. Five extramural sites were funded. Together with the CDC, they will implement the SEED 3 collaborative protocol. The SEED 3 protocol for identification of study participants, recruitment, and study data collection flow will be similar to the protocols for SEED 1 and 2.
However, while all SEED phases have the same research goals and the same basic study design, data collection has been greatly streamlined and revised between SEED 1, SEED 2, and SEED 3. Many study instruments and data collection components included in the SEED 1 protocol are not included in the SEED 3 protocol; two instruments included in the SEED 3 protocol were developed subsequent to SEED 1 to capture an abbreviated version of information that had been included on some of the discontinued SEED 1 forms and to capture some additional information overlooked in the SEED 1 protocol; and instruments included in all phases of SEED underwent review and minor revision subsequent to SEED 1 to address ambiguities and difficulties experienced during SEED 1 data collection. Implementing this phase of SEED will increase the total SEED pooled sample size for investigation of high priority hypotheses. Maintaining the same basic study design and general protocol integrity will ensure that data pooling can be achieved across SEED phases.
Families will be identified from each of the 3 groups: Autism Spectrum Disorder (ASD), other developmental delay or disorder comparison group (DD), and a second comparison group of children randomly drawn from the entire study cohort population (POP). It is expected that the 6 SEED 3 study sites will have a total of 2,106 children enroll and complete the study protocol. The data collection process will take approximately 9 hours 10 minutes (ASD group); 5 hours 30 minutes (POP group); 2 hours 45 minutes (DD group) to complete, which includes (1) maternal telephone interview with questions about maternal reproductive history and Start Printed Page 71506pregnancy with the index child, (2) parent-completed questionnaires about parental and child health and child development, (3) in-person child developmental evaluation, (4) maternal and child anthropometry measurements, and (5) biosampling from biological parents and child.
There are no costs to participants other than their time. The total estimated annual burden hours are 7,118.
|Type of respondents||Form name||Number of respondents||Number responses per respondent||Average burden per response (in hours)|
|Mother All potential participants sent mailing||Invitation Packet/Response Card||1,718||1||10/60|
|Mother Potentially eligible with contact by study staff||Invitation Call Script and Social Communication Questionnaire||859||1||30/60|
|Mother Eligible, consented, and enrolled; assigned to the ASD workflow based on enrollment intake||Enrollment Packet||469||1||20/60|
|Mother Completed this study step||Follow-up Phone Call Script and Pregnancy Reference Form||422||1||15/60|
|Maternal Interview Call||422||1||1|
|Follow-up Call 2||375||1||20/60|
|Clinic/Home Visit—Developmental Assessment||328||1||225/60|
|Father Completed this study step||Clinic/Home Visit—Saliva Collection (optional—on own)||164||1||15/60|
|Child Completed this study step||Clinic/Home Visit—Developmental Assessment||328||1||135/60|
|Mother All potential participants sent mailing||Invitation Packet/Response Card||1,466||1||10/60|
|Mother Potentially eligible with contact by study staff||Invitation Call Script and Social Communication Questionnaire||733||1||30/60|
|Mother Eligible, consented, and enrolled; assigned to the POP workflow based on enrollment intake||Enrollment Packet||334||1||20/60|
|Mother Completed this study step||Follow-up Phone Call Script and Pregnancy Reference Form||301||1||15/60|
|Maternal Interview Call||301||1||1|
|Follow-up Call 2||267||1||20/60|
|Clinic/Home Visit—Developmental Assessment||234||1||50/60|
|Father Completed this study step||Clinic/Home Visit—Saliva Collection (optional—on own)||117||1||15/60|
|Child Completed this study step||Clinic/Home Visit—Developmental Assessment||234||1||90/60|
|Mother All potential participants sent mailing||Invitation Packet/Response Card||641||1||10/60|
|Mother Potentially eligible with contact by study staff||Invitation Call Script and Social Communication Questionnaire||321||1||30/60|
|Mother Eligible, consented, and enrolled; assigned to the DD workflow based on enrollment intake||Enrollment Packet||175||1||20/60|
|Mother Completed this study step||Follow-up Phone Call Script and Pregnancy Reference Form||158||1||15/60|
|Maternal Interview Call||158||1||1|
|Follow-up Call 2||140||1||20/60|
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention.
[FR Doc. 2016-25061 Filed 10-14-16; 8:45 am]
BILLING CODE 4163-18-P