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App I_Final Survey for Boot Wear Evaluation

ICR 201906-0920-012 · OMB 0920-1125 · Object 92835801.

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application/vnd.openxmlformats-officedocument.wordprocessingml.document
App I_Final Survey for Boot Wear Evaluation
Foley, Tamekia (CDC/NIOSH/OD)
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2016-05-17
2026-09-20
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						Appendix I										
                                    Final Survey for Boot Wear Evaluation















































											

											Form Approved
											OMB No. 0920-XXXX
											Exp. Date xx/xx/20xx

                                                  



				 Final Survey for Boot Wear Evaluation

Assigned participant ID: __________
Date: ____ / _____ / 20 _____
Recorded by:  MFN / MEN / PD / WP / JP / AM / JM
Picture of boots taken:  Yes  /  No 	Scan of boots taken:  Yes  /  No

1.	What is your reason for ending this study? 
	My company decided that I needed to replace my boots. 
	This is the normal time for company-wide/site wide/crew wide replacement
	I decided I no longer wanted to participate. 
	I decided that the boots had reached the end of their usable life
	How did you decide the boots had reached the end of their usable life? 
____________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________
2.	Were your boots returned to the researcher? Yes  /  No
3.	If you had a choice of wearing this exact make and model of boot again, would you?
	Yes, I hope to get these boots again. 
	Yes, I would wear them again.
	No, I would not wear them again. 
	Please explain: ____________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________________







CDC estimates the average public reporting burden for this collection of information as 5 minutes per response, including the time for reviewing instructions, searching existing data/information sources, gathering and maintaining the data/information 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 CDC/ATSDR Information Collection Review Office, 1600 Clifton Road NE, MS D-74, Atlanta, Georgia 30333; ATTN: PRA (0920-XXXX).