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DOCUMENT ID: [30Day-11-04]
SUBJECT CATEGORY: Proposed Data Collections Submitted for Public Comment and Recommendations
DOCUMENT SUMMARY:
The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 4981210. Send written comments to CDC, Desk Officer, Human Resources and Housing Branch, New Executive Office Building, Room 10235, Washington, DC 20503 or by fax to (202) 3956974. Written comments should be received within 30 days of this notice.
Proposed Project: Families, Communities, and Diabetes Management ProjectNewNational Center for Chronic Disease Prevention
[[Page 70799]]
and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC).
Diabetes Mellitus Type 2 is a chronic metabolic disease that has the potential for serious health consequences which include both psychological and physical conditions. Effective management of this disease is important to prevent the development of these problems. No previous studies have systematically examined the ways in which psychological functioning, patientprovider relationships, family and social support, health insurance availability and utilization, lifestyle practices, and community support influence diabetes self management among African American patients. Most diabetes management information is based on research conducted primarily with Caucasian patients. The Division of Diabetes Translation within the National Center for Chronic Disease Prevention and Health Promotion of the Centers for Disease Control and Prevention plans to conduct a pilot study of a longitudinal, familycentered research project to determine optimal ways of teaching African American patients and their families how to work together to manage diabetes successfully.
The research will involve samples of 40to 64yearold African American men and women with Type 2 diabetes and their close family members. Participating families will be divided into two groups, an intervention group that will receive the intervention at the beginning of the study, and a comparison group that will receive a modified version at the end. Measurements of selfcare adherence and diabetes control will include both selfreports and objective measures such as blood glucose levels obtained through clinical lab work. Other data will include diabetes knowledge, community characteristics, social support, community support, psychological functioning, patientprovider relationships, and health care coverage. Participant involvement will occur over a 13 month period.
CDC is requesting a three year approval for this data collection.
The estimated annualized burden is 1,433 hours. The total burden over the course of this data collection is 4,300 hours.
Number of Average burden
Respondents Number of responses per per response
respondents respondent (in hours) Adults with Diabetes:
Questionnaires.............................................. 400 3 1
Clinical Lab Work........................................... 400 3 1
Glucose Test Meter Training................................. 400 1 1 Family Members: Questionnaires.................................. 400 3 45/60 Teenagers: Questionnaires....................................... 400 3 30/60
Dated: December 9, 2003.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease Control and Prevention.
[FR Doc. 0331307 Filed 121803; 8:45 am]
BILLING CODE 416318P
SUMMARY: Agency information collection activities; proposals, submissions, and approvals,
DOCUMENT BODY 2:
The Centers for Disease Control and Prevention (CDC) publishes a list of information collection requests under review by the Office of Management and Budget (OMB) in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these requests, call the CDC Reports Clearance Officer at (404) 4981210. Send written comments to CDC, Desk Officer, Human Resources and Housing Branch, New Executive Office Building, Room 10235, Washington, DC 20503 or by fax to (202) 3956974. Written comments should be received within 30 days of this notice.
Proposed Project: Families, Communities, and Diabetes Management ProjectNewNational Center for Chronic Disease Prevention
[[Page 70799]]
and Health Promotion (NCCDPHP), Centers for Disease Control and Prevention (CDC).
Diabetes Mellitus Type 2 is a chronic metabolic disease that has the potential for serious health consequences which include both psychological and physical conditions. Effective management of this disease is important to prevent the development of these problems. No previous studies have systematically examined the ways in which psychological functioning, patientprovider relationships, family and social support, health insurance availability and utilization, lifestyle practices, and community support influence diabetes self management among African American patients. Most diabetes management information is based on research conducted primarily with Caucasian patients. The Division of Diabetes Translation within the National Center for Chronic Disease Prevention and Health Promotion of the Centers for Disease Control and Prevention plans to conduct a pilot study of a longitudinal, familycentered research project to determine optimal ways of teaching African American patients and their families how to work together to manage diabetes successfully.
The research will involve samples of 40to 64yearold African American men and women with Type 2 diabetes and their close family members. Participating families will be divided into two groups, an intervention group that will receive the intervention at the beginning of the study, and a comparison group that will receive a modified version at the end. Measurements of selfcare adherence and diabetes control will include both selfreports and objective measures such as blood glucose levels obtained through clinical lab work. Other data will include diabetes knowledge, community characteristics, social support, community support, psychological functioning, patientprovider relationships, and health care coverage. Participant involvement will occur over a 13 month period.
CDC is requesting a three year approval for this data collection.
The estimated annualized burden is 1,433 hours. The total burden over the course of this data collection is 4,300 hours.
Number of Average burden
Respondents Number of responses per per response
respondents respondent (in hours) Adults with Diabetes:
Questionnaires.............................................. 400 3 1
Clinical Lab Work........................................... 400 3 1
Glucose Test Meter Training................................. 400 1 1 Family Members: Questionnaires.................................. 400 3 45/60 Teenagers: Questionnaires....................................... 400 3 30/60
Dated: December 9, 2003.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease Control and Prevention.
[FR Doc. 0331307 Filed 121803; 8:45 am]
BILLING CODE 416318P
14 CFR Part 39 40 CFR Part 52 14 CFR Part 71 33 CFR Part 165 50 CFR Part 679 47 CFR Part 73 26 CFR Part 1 40 CFR Part 180 33 CFR Part 117 50 CFR Part 17 44 CFR Part 67 50 CFR Part 648 14 CFR Part 97 33 CFR Part 100 40 CFR Part 63 50 CFR Part 622 44 CFR Part 65 50 CFR Part 660 26 CFR Part 301 39 CFR Part 111 40 CFR Part 300 6 CFR Part 5 40 CFR Part 271 47 CFR Part 64 40 CFR Parts 52 and 81 50 CFR Part 665 44 CFR Part 64 10 CFR Part 50 49 CFR Part 571 47 CFR Part 76