[NCIPC] The National Intimate Partner and Sexual Violence Survey (NISVS)
Revision of a currently approved collection
Yes
Regular
Approved with change
05/09/2023
02/16/2023
The redesign of the NISVIS is approved for fielding the 2023-2024 cycle of data collection. Before the program launches a second cycle of the redesigned NISVIS, the program must brief OMB on response rates from the first cycle, and whether there continues to be a relationship between increasing response and decreasing prevalence in intimate violence outcomes found in the pilot persists, their assessment of whether the increased response is driven more by the personal outreach to respondents vs. the larger incentive, and provide the text it will use on its website to discuss the impact of the break in series from the new design on how the public should interpret longitudinal trends in intimate violence rates. Depending upon the additional changes that the program requests for the second cycle of the redesign, OMB will advise whether a Revision vs a Nonsub Change Request should be submitted.
table that charts list comparision
Inventory as of this Action
Requested
Previously Approved
05/31/2026
36 Months From Approved
05/31/2023
211,067
0
534
17,949
0
101
0
0
2,676
The National Intimate Partner and Sexual Violence Survey is an ongoing, nationally representative survey of non-institutionalized adult men and women aged 18 years or older in the United States assessing lifetime experiences to assess experiences of intimate partner violence, sexual violence and stalking among adults in the US. . It measures lifetime victimization for these types of violence as well as in the previous 12 months. NISVS has historically been administered through random-digit-dial sampling. From 2018-2021, CDC conducted feasibility testing and pilot testing aimed at developing methods for transitioning NISVS to an address-based sampling design that would reduce reliance on cell and landline phone participation and improve response rates. The modification in this revision request is to do a full-scale implementation of address-based sampling frame with push-to-web data collection and a call-in telephone option, intended to increase the response rate, and reduce respondent burden.
US Code:
42 USC 241
Name of Law: Public Health Service Act
The sample size was substantially reduced during the redesign and pilot testing phase (i.e., sampled fewer respondents). The current request ramps the sample back up in conjunction with implementing the changes made during the redesign and testing phase. The estimated burden in this revision is higher than that the previously approved burden. The total burden increase for this revision is due to the changes made in sampling and survey methods. Note that the reduction in "cost" burden is due to a change in the method of calculation, not a difference in cost (CDC is adopting the HHS method of calculation in all of their packages.)
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
Form 0920-0822 Att L_Web_Phone Screeners and Survey Instrument_Spanish
NISVS Change Request 04JUN2021.docx
IRB Approval.pdf
Questionnaire, phone (Att. K-L)