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2021 NLM ClinicalTrials.gov Usability Testing Survey (NLM)
Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery (NIH)
OMB: 0925-0648
IC ID: 246050
OMB.report
HHS/NIH
OMB 0925-0648
ICR 202104-0925-001
IC 246050
( )
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0925-0648 can be found here:
2024-06-25 - Extension without change of a currently approved collection
2023-08-25 - No material or nonsubstantive change to a currently approved collection
Documents and Forms
Document Name
Document Type
Form 1
2021 NLM ClinicalTrials.gov Usability Testing Survey (NLM)
Form
1 2021 ClinicalTrials.gov User Sign-up
NLM 2021 ClinicalTrials.gov User Sign-Up Instrument..pdf
Form
1 2021 ClinicalTrials.gov User Sign-up
NLM 2021 ClinicalTrials.gov User Sign-Up Instrument..pdf
Form
2 2021 ClinicalTrials.gov Usability Study survey
NLM 2021 ClinicalTrials.gov Usability Study Survey Instrument.pdf
Form and Instruction
2 2021 ClinicalTrials.gov Usability Study survey
NLM 2021 ClinicalTrials.gov Usability Study Survey Instrument.pdf
Form and Instruction
NLM Fast Track ICR_2021 ClinicalTrials.gov Usability Testing.docx
fast track study NLM 2021 ClinicalTrials.gov Usability Testing
IC Document
NLM Fast Track ICR_2021 ClinicalTrials.gov Usability Testing.docx
fast track study NLM 2021 ClinicalTrials.gov Usability Testing
IC Document
Information Collection (IC) Details
View Information Collection (IC)
IC Title:
2021 NLM ClinicalTrials.gov Usability Testing Survey (NLM)
Agency IC Tracking Number:
IC Status:
Unchanged
Obligation to Respond:
Voluntary
CFR Citation:
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Form
1
2021 ClinicalTrials.gov User Sign-up
NLM 2021 ClinicalTrials.gov User Sign-Up Instrument..pdf
Yes
Yes
Fillable Fileable
Form and Instruction
2
2021 ClinicalTrials.gov Usability Study survey
NLM 2021 ClinicalTrials.gov Usability Study Survey Instrument.pdf
No
Paper Only
Federal Enterprise Architecture Business Reference Module
Line of Business:
Health
Subfunction:
Health Care Services
Privacy Act System of Records
Title:
FR Citation:
Number of Respondents:
60
Number of Respondents for Small Entity:
0
Affected Public:
Individuals or Households
Percentage of Respondents Reporting Electronically:
0 %
Requested
Program Change Due to New Statute
Program Change Due to Agency Discretion
Change Due to Adjustment in Agency Estimate
Change Due to Potential Violation of the PRA
Previously Approved
Annual Number of Responses for this IC
60
0
0
0
0
60
Annual IC Time Burden (Hours)
42
0
0
0
0
42
Annual IC Cost Burden (Dollars)
0
0
0
0
0
0
Documents for IC
Title
Document
Date Uploaded
fast track study NLM 2021 ClinicalTrials.gov Usability Testing
NLM Fast Track ICR_2021 ClinicalTrials.gov Usability Testing.docx
03/01/2021
Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.