OMB #: 0925-0593
OMB Expiration Date: 8/31/2014
Breast Milk SAQ, Phase 2g
OMB Specification
Breast Milk SAQ
Event Category: |
Time-Based |
Event: |
Birth, 3M |
Administration: |
N/A |
Instrument Target: |
Biological Mother |
Instrument Respondent: |
Biological Mother |
Domain: |
Biospecimen |
Document Category: |
Sample Collection |
Method: |
Self-Administered |
Mode (for this instrument*): |
In-Person, PAPI |
OMB Approved Modes: |
In-Person, PAPI; |
Estimated Administration Time: |
40 minutes |
Multiple Child/Sibling Consideration: |
Per Event |
Special Considerations: |
N/A |
Version: |
2.0 |
MDES Release: |
4.0 |
*This instrument is OMB-approved for multi-mode administration but this version of the instrument is designed for administration in this/these mode(s) only.
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Breast Milk SAQ
TABLE OF CONTENTS
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Breast Milk SAQ
WHEN PROGRAMMING INSTRUMENTS, VALIDATE FIELD LENGTHS AND TYPES AGAINST THE MDES TO ENSURE DATA COLLECTION RESPONSES DO NOT EXCEED THOSE OF THE MDES. SOME GENERAL ITEM LIMITS USED ARE AS FOLLOWS:
DATA ELEMENT FIELDS |
MAXIMUM CHARACTERS PERMITTED |
DATA TYPE |
PROGRAMMER INSTRUCTIONS |
ADDRESS AND EMAIL FIELDS |
100 |
CHARACTER |
|
UNIT AND PHONE FIELDS |
10 |
CHARACTER |
|
_OTH AND COMMENT FIELDS |
255 |
CHARACTER |
|
FIRST NAME AND LAST NAME |
30 |
CHARACTER |
|
ALL ID FIELDS |
36 |
CHARACTER |
|
ZIP CODE |
5 |
NUMERIC |
|
ZIP CODE LAST FOUR |
4 |
NUMERIC |
|
CITY |
50 |
CHARACTER |
|
DOB AND ALL OTHER DATE FIELDS (E.G., DT, DATE, ETC.) |
10 |
NUMERIC
CHARACTER
|
MM MUST EQUAL 01 TO 12 DD MUST EQUAL 01 TO 31 YYYY MUST BE BETWEEN 1900 AND CURRENT YEAR. |
TIME VARIABLES |
TWO-DIGIT HOUR AND TWO-DIGIT MINUTE, AM/PM DESIGNATION |
NUMERIC |
HOURS MUST BE BETWEEN 00 AND 12; MINUTES MUST BE BETWEEN 00 AND 59 |
Instrument Guidelines for Participant and Respondent IDs:
PRENATALLY, THE P_ID IN THE MDES HEADER IS THAT OF THE PARTICIPANT (E.G. THE NON-PREGNANT WOMAN, PREGNANT WOMAN, OR THE FATHER).
POSTNATALLY, A RESPONDENT ID WILL BE USED IN ADDITION TO THE PARTICIPANT ID BECAUSE SOMEBODY OTHER THAN THE PARTICIPANT MAY BE COMPLETING THE INTERVIEW. FOR EXAMPLE, THE PARTICIPANT MAY BE THE CHILD AND THE RESPONDENT MAY BE THE MOTHER, FATHER, OR ANOTHER CAREGIVER. THEREFORE, MDES VERSION 2.2 AND ALL FUTURE VERSIONS CONTAIN A R_P_ID (RESPONDENT PARTICIPANT ID) HEADER FIELD FOR EACH POST-BIRTH INSTRUMENT. THIS WILL ALLOW ROCs TO INDICATE WHETHER THE RESPONDENT IS SOMEBODY OTHER THAN THE PARTICIPANT ABOUT WHOM THE QUESTIONS ARE BEING ASKED.
A REMINDER:
ALL RESPONDENTS MUST BE CONSENTED AND HAVE RECORDS IN THE PERSON, PARTICIPANT, PARTICIPANT_CONSENT AND LINK_PERSON_PARTICIPANT TABLES, WHICH CAN BE PRELOADED INTO EACH INSTRUMENT. ADDITIONALLY, IN POST-BIRTH QUESTIONNAIRES WHERE THERE IS THE ABILITY TO LOOP THROUGH A SET OF QUESTIONS FOR MULTIPLE CHILDREN, IT IS IMPORTANT TO CAPTURE AND STORE THE CORRECT CHILD P_ID ALONG WITH THE LOOP INFORMATION. IN THE MDES VARIABLE LABEL/DEFINITION COLUMN, THIS IS INDICATED AS FOLLOWS: EXTERNAL IDENTIFIER: PARTICIPANT ID FOR CHILD DETAIL.
BMD01000. As part of the National Children’s Study, we are asking you to provide a breast milk sample from one breast. Please follow the instructions provided in the breast milk collection kit to collect the sample.
After you have collected the breast milk sample, please complete the information on both sides of this form.
BMD02000. On what date did you collect the sample?
SOURCE |
National Children’s Study, Legacy Phase (Modified) (1M & 6M) |
(P_BMQ_MM) |___|___|
M M
(P_BMQ_DD) |___|___|
D D
(P_BMQ_YYYY) |___|___|___|___|
Y Y Y Y
BMD03000. At what time did you collect the sample?
SOURCE |
National Children’s Study, Legacy Phase (Modified) (1M & 6M) |
(P_BMQ_TIME) l___l___l : l___l___l
H H M M
(P_BMQ_TIME_UNIT)
Label |
Code |
Go To |
AM |
1 |
|
PM |
2 |
|
BMD04000/(P_BMQ_HOW_LONG). How long did it take you to collect this sample?
Label |
Code |
Go To |
0 - 10 minutes |
1 |
|
11 - 20 minutes |
2 |
|
Over 20 minutes |
3 |
|
SOURCE |
National Children’s Study, Vanguard Phase |
BMD05000/(P_BMQ_LAST_FEED). How long before collecting the breast milk sample did you last breast-feed your baby or pump milk from this breast?
Label |
Code |
Go To |
Less than 2 hours |
1 |
|
2-4 hours |
2 |
|
Over 4 hours |
3 |
|
SOURCE |
National Children’s Study, Legacy Phase (Modified) (1M & 6M) |
BMD06000/(P_BMQ_PUMP). Did you use a pump to collect the sample?
Label |
Code |
Go To |
Yes |
1 |
|
No |
2 |
P_BMQ_EMPTY |
SOURCE |
National Children’s Study, Vanguard Phase |
BMD07000/(P_BMQ_TYPE_PUMP). What type of pump did you use to collect the sample?
Label |
Code |
Go To |
Electric pump |
1 |
|
Hand pump |
2 |
|
SOURCE |
National Children’s Study, Vanguard Phase |
BMD08000/(P_BMQ_BRAND_PUMP). What is the brand of the pump you used to collect the sample? (Mark one)
Label |
Code |
Go To |
Medela® |
1 |
P_BMQ_EMPTY |
AVENT® |
2 |
P_BMQ_EMPTY |
Playtex® |
3 |
P_BMQ_EMPTY |
Ameda® |
4 |
P_BMQ_EMPTY |
Evenflo® |
5 |
P_BMQ_EMPTY |
Lansinoh® |
6 |
P_BMQ_EMPTY |
Other |
-5 |
|
Don't Know |
-2 |
P_BMQ_EMPTY |
SOURCE |
National Children’s Study, Vanguard Phase |
BMD09000/(P_BMQ_BRAND_PUMP_OTH). SPECIFY: _________________________________________
SOURCE |
National Children’s Study, Vanguard Phase |
BMD10000/(P_BMQ_EMPTY). Did you completely empty the breast when collecting the sample?
Label |
Code |
Go To |
Yes |
1 |
|
No |
2 |
|
Don't Know |
-2 |
|
SOURCE |
National Children’s Study, Vanguard Phase |
BMD11000/(P_BMQ_CAFFEINE). During the 2 hours prior to collecting the breast milk sample, did you eat or drink any food or beverage containing caffeine (for example, coffee, tea, soda, chocolate)?
Label |
Code |
Go To |
Yes |
1 |
|
No |
2 |
|
SOURCE |
National Children’s Study, Vanguard Phase |
BMD12000/(P_BMQ_ALCOHOL). During the 2 hours prior to collecting the breast milk sample, did you drink any alcohol?
Label |
Code |
Go To |
Yes |
1 |
|
No |
2 |
|
SOURCE |
National Children’s Study, Vanguard Phase |
BMD13000. Please write down the name of any prescription, over-the-counter, homeopathic, or non-traditional medicines you have taken in the last 24 hours (including prenatal vitamins). Please be specific. For example, if you took Robitussin DM®, write Robitussin DM®, not Robitussin®. If you did not take any prescription or over-the-counter medications in the last 24 hours, please mark None.
SOURCE |
National Children’s Study, Vanguard Phase |
(P_BMQ_PRSC_OTC_1) _________________________________________________________
Label |
Code |
Go To |
None |
1 |
P_BMQ_FREEZER |
(P_BMQ_PRSC_OTC_2) ______________________________________________________
(P_BMQ_PRSC_OTC_3) ____________________________________________________________
(P_BMQ_PRSC_OTC_4) _________________________________________________
(P_BMQ_PRSC_OTC_5) _________________________________________________
(P_BMQ_PRSC_OTC_6) _____________________________________________________
(P_BMQ_PRSC_OTC_7) _______________________________________________
(P_BMQ_PRSC_OTC_8) _______________________________________________
(P_BMQ_PRSC_OTC_9) ___________________________________________
(P_BMQ_PRSC_OTC_10) __________________________________________
BMD14000/(P_BMQ_FREEZER). How long after collecting your sample did you place it in the freezer?
Label |
Code |
Go To |
0-10 minutes |
1 |
|
11-20 minutes |
2 |
|
Over 20 minutes |
3 |
|
Not Applicable (did not place in freezer) |
-7 |
|
SOURCE |
National Children’s Study, Legacy Phase (Modified) (1M & 6M) |
BMD15000. Thank you for participating in the National Children’s Study and for taking the time to complete this information.
Please call the Regional Operations Center number located on the last page, if you have any questions.
FOU01000/(SPECIMEN_ID). Specimen ID:
l__l__l__l__l__l__l__l__l__l - l__l__l__l__l
FOU02000/(P_ID). Participant ID:_________________________________
FOU03000/(R_P_ID). Respondent ID:______________________________________
FOU04000/(EVENT_ID). Visit Type/Event ID:_________________________________________
Public reporting burden for this collection of information is estimated to average 40 minutes per response, including the time for reviewing instructions, searching existing data sources, gathering and maintaining the data needed, and completing and reviewing the collection of information. An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. Send comments regarding this burden estimate or any other aspect of this collection of information, including suggestions for reducing this burden, to: NIH, Project Clearance Branch, 6705 Rockledge Drive, MSC 7974, Bethesda, MD 20892-7974, ATTN: PRA (0925-0593*). Do not return the completed form to this address.
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
File Modified | 0000-00-00 |
File Created | 2021-01-28 |