NYTD TA Brief #5 - Designing an Informed Consent Form for Use with the Youth Outcome Survey

Technical Assistance Brief No. 5
Issued: August 2010

Designing an Informed
Consent Form for Use with
the Youth Outcome Survey

In this brief:
We provide an overview of the
informed consent process and
discuss strategies for
documenting this process using
an informed consent form with
the NYTD youth outcome
survey.

Concern about the possible exploitation of adults
and children in research studies has led to the
development of federal policy designed to protect
Target audience: Independent
human research subjects. This federal policy is
living coordinators
established at 45 CFR 46
(http://www.hhs.gov/ohrp/humansubjects/guidance/4
Key words: Informed consent and
assent; youth outcome survey
5cfr46.htm). One of the main elements of the
federal policy is the requirement to seek informed
consent from research subjects. Informed consent is a process of sharing information
between the investigator and the prospective research subject that will assist the subject
in making an informed decision about whether or not to participate in the research. For
most research, informed consent is documented using a written form that provides key
information regarding the research. This Technical Assistance Brief, focused on the
design of the informed consent form, is the first in a series of briefs on the topic of
informed consent.
The data collection required by NYTD is not considered a research activity that is subject
to the federal regulations for the protection of human subjects. Therefore, there is no
specific federal requirement or procedure to seek informed consent of a youth, or
parental consent on a youth's behalf, to participate in the NYTD youth outcome survey
(see NYTD Question and Answer #3.18 at
http://www.acf.hhs.gov/programs/cb/systems/nytd/faq/). However, states are
encouraged to develop their own procedures to ensure that youth understand the
purpose and use of the survey, including the voluntary nature of the survey. A consent
form not only explains the study to the youth but gives youth clear decision-making
authority regarding their participation, and if worded in a youth friendly manner, may
actually assist in garnering the participation of youth in the NYTD survey.
We recommend that states develop a simple consent form (or, for youth under 18, an
“assent” form) to accompany the youth outcome survey that explains the purpose of the
survey, how the data will be collected and used, and that participation in the survey is
voluntary. Youth may be asked to sign the form at the bottom or check a box indicating
that they understand the information presented and agree to participate. Depending on
the state’s survey mode, the consent form may be accessed on the web, presented on
paper, or administered over the telephone.

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TA Brief No. 5: Obtaining Informed Consent for Participation in the Youth Outcome Survey

A well designed consent form serves multiple purposes. It informs participants of their rights, it
reassures respondents regarding the purpose and length of the survey, and it notifies
participants about the need to stay in touch for the follow-up surveys. If a state decides to
provide a consent form to youth it is recommended that the form cover the following areas as
they relate to NYTD (adapted from HHS regulations 45 CFR 46.116(a)):

▪
▪
▪
▪

▪
▪

▪

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Why the survey is being conducted. A brief explanation might note that NYTD is
being conducted in all states to collect information on how youth leaving foster care are
doing.
Who is being asked to complete the survey. The explanation should say that all
youth in foster care who are turning age 17 during a certain federal Fiscal Year are being
surveyed nationally and will be surveyed again at ages 19 and 21.
How the data will be used. The state may note that the data will be used to evaluate
and improve programs that help foster youth become independent adults. If the state
has specific plans for how the data will be used, this might also be discussed.
The benefits of participation. States that are offering an incentive should state what
type of incentive is being offered and the amount of the incentive (i.e., cash or a gift
card). Other benefits that might be discussed are the opportunity for youth to share their
experiences and contribute to the improvement of the services for themselves and other
youth transitioning from care.
How long it will take (on average) for the youth to complete the survey. States
should provide youth an accurate estimate of how long the survey will take based on
pilot testing completed in the state or by other states.
That the survey is voluntary. Youth need to know that their participation is voluntary
and that there will be no penalty (such as a loss of services) if they choose not to
participate. Youth should also be informed that they can decline to respond to any
questions that they do not want to answer.
Confidentiality procedures. It is important for youth to know who will see their
answers and whether their data will be confidential. In some states, all data will be
associated with an ID number and very few individuals will have access to the file that
links the ID with a youth’s name. Other states may be planning to use the youth’s data
to offer needed services when the youth discloses certain problems on the survey, such
as being homeless. Youth should be informed about which procedure will be followed
for their data. All youth should be advised that their data will never be published with
their identification associated with their responses.
A place to go for more information. The consent form should provide a telephone
number that youth can call if they have questions about the survey.

The consent form should be written in simple language that is easily understood by the youth.
Youth should also receive their own copy of the consent form in case they later have questions
about the study and their participation.

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TA Brief No. 5: Obtaining Informed Consent for Participation in the Youth Outcome Survey

In the next brief on informed consent, we will discuss strategies for implementing an informed
consent process using a state example.
Additional information on informed consent is provided by these sources:
•
•
•

Federal Office for Human Research Protections (OHRP) (www.hhs.gov/ohrp).
45 CFR 46: Protection of Human Subjects
(http://www.hhs.gov/ohrp/humansubjects/guidance/45cfr46.htm)
Office for Human Research Protection’s Tips on Informed Consent
(http://www.hhs.gov/ohrp/humansubjects/guidance/ictips.htm).

For more information, please contact:
NYTDinfo@acf.hhs.gov

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