- From: Jeanne Spellman <jspellman@spellmanconsulting.com>
- Date: Tue, 30 Apr 2019 11:15:39 -0400
- To: Silver Task Force <public-silver@w3.org>
- Message-ID: <781176ad-0c71-f4b9-3a6e-9534c5a0cb11@spellmanconsulting.com>
== HTML Minutes: ==
https://www.w3.org/2019/04/30-silver-minutes.html
Note that the topics are not correct in the HTML minutes: The first
topic was the Requirements: Technology Neutral re-wording. I have fixed
it in the text version of the minutes below, but could not fix it in the
HTML version.
== Summary of Resolutions ==
Summary of Resolutions
1. Technology Neutral: Guidance should be expressed in generic terms so that
they may apply to more than one platform or technology. The
intent of technology-neutral wording is to provide the
opportunity to apply the core guidelines to current and
emerging technology, even if specific technical advice
doesn't yet exist.
== Text Version of Minutes ==
[1]W3C
[1] http://www.w3.org/
- DRAFT -
Silver Community Group Teleconference
30 Apr 2019
Attendees
Present
Lauriat, jeanne, JF, ChrisLoiselle, Makoto, Chuck, Shri,
KimD, kirkwood, Cyborg, Rachael
Regrets
Bruce, Denis, Angela
Chair
Shawn, jeanne
Scribe
jeanne
Contents
* [2]Topics
1. [3]Requirements: Technology Neutral rewording
2. [5]AccessU
3. [6]Design PRinciple 9
4. [7]Requirements: Technology Neutral
* [8]Summary of Action Items
* [9]Summary of Resolutions
__________________________________________________________
Requirements: Technology Neutral rewording
<scribe> scribe: jeanne
Shawn: We left off with Technology Neutral
<Lauriat>
[10]https://w3c.github.io/silver/requirements/#technology-neutr
al
[10] https://w3c.github.io/silver/requirements/#technology-neutral
jeanne: We were asked to bring it in line with WCAG 2
Requirements [11]https://www.w3.org/TR/wcag2-req/
[11] https://www.w3.org/TR/wcag2-req/
Shawn: It is also too specific in how - Guidelines and Methods
Guidance should be expressed in generic terms so that they may
apply to more than one platform or technology.
jeanne: The above was the most recent proposal from Friday
[discussion recapping proposals]
<Lauriat>
[12]https://w3c.github.io/silver/requirements/#technology-neutr
al
[12] https://w3c.github.io/silver/requirements/#technology-neutral
<JF> Core guidelines are user-centric. Methods are
technology-centric. The core guidelines are worded to apply
across varied technologies and avoid being technology-specific.
The intent of technology-neutral wording is to provide the
opportunity to apply the core guidelines to current and
emerging technology, even if the technical advice doesn't yet
exist. Technical details are discoverable in the Methods but
are not required to understand guidelines.
<Lauriat> Guidance should be expressed in generic terms so that
they may apply to more than one platform or technology. The
intent of technology-neutral wording is to provide the
opportunity to apply the core guidelines to current and
emerging technology, even if the technical advice doesn't yet
exist.
<KimD> +1 it's very close to 2.0 and I'm fine replacing the
current with the new short.
<Lauriat> Guidance should be expressed in generic terms so that
they may apply to more than one platform or technology. The
intent of technology-neutral wording is to provide the
opportunity to apply the core guidelines to current and
emerging technology, even if specific technical advice doesn't
yet exist.
jeanne: I like including the second sentence.
JF: "Specific technical advice"
... it's clearer than the original.
<kirkwood> +1
<kirkwood> seems clear to me
<Makoto> +1 to "Specific technical advice"
<Chuck> +1
Shawn: ANd it avoids saying Guidelines and Methods
<KimD> +1
<ChrisLoiselle> +1
+1
<Shri> What is the difference "technology" and "platform?"
<Cyborg> the phone number code isn't working...
Shawn: Not a huge difference. Technology is what you creating
something in or with: like HTML, java, XML, CSS. The platform
is the operating system.
JF: agree with Shawn
<Cyborg> sorry, it's ok, figured it out - in now
RESOLUTION: Guidance should be expressed in generic terms so
that they may apply to more than one platform or technology.
The intent of technology-neutral wording is to provide the
opportunity to apply the core guidelines to current and
emerging technology, even if specific technical advice doesn't
yet exist.
<Cyborg> link again please if you can
<Lauriat>
[13]https://w3c.github.io/silver/requirements/#technology-neutr
al
[13] https://w3c.github.io/silver/requirements/#technology-neutral
<Cyborg> +1 to that
<Cyborg> what is the concern about design principle 9?
<Lauriat>
[14]https://w3c.github.io/silver/requirements/#design-principle
s
[14] https://w3c.github.io/silver/requirements/#design-principles
<KimD> It's under §2
<Cyborg> let's wait
<Jan> I am having trouble connecting to the audio and webex.
<Jan> Here is the text I came up with as a part of my homework
from last week:
<Jan> Be data-informed and evidence-based, recognizing that
research outcomes may come from small sample sizes due to the
prevalence of certain types of disabilities. Research-based
recommendations for large groups of people with disabilities
should not override recommendations that are made for smaller
groups. The intent is to make informed decisions wherever
possible and to ensure that the needs of all disability
categories are effectively represented. This means that
AccessU
<Jan> I will continue to try....
Jeanne: We have a room at AccessU for Wed, Thurs and Friday. I
will also be there MOnday and Tuesday if anyone wants to get
together .
Design PRinciple 9
<Cyborg> the problem with the audio on my end is that i was
using an old email from April 19 that somehow other people
responded to with regrets more recently.
Be data-informed and evidence-based, recognizing that research
outcomes may come from small sample sizes due to the prevalence
of certain types of disabilities. Research-based
recommendations for large groups of people with disabilities
should not override recommendations that are made for smaller
groups. The intent is to make informed decisions wherever
possible and to ensure that the needs
of all disability categories are effectively represented. This
means that
<Cyborg> Jan - check heading of your email - for April 30
<Jan> This means that new Methods submitted by the public could
require user research test results to verify validity. When in
doubt, see Design Principle 1.
<Cyborg> she just added more
Be data-informed and evidence-based, recognizing that research
outcomes may come from small sample sizes due to the prevalence
of certain types of disabilities. Research-based
recommendations for large groups of people with disabilities
should not override recommendations that are made for smaller
groups. The intent is to make informed decisions wherever
possible and to ensure that the needs
of all disability categories are effectively represented. This
means that new Methods submitted by the public could require
user research test results to verify validity. When in doubt,
see Design Principle 1.
<Jan> Thanks, John ... trying that.
jeanne: I like it without the last two sentences.
Cybele: I want to work on the phrasing of the small sample
sizes, It's not always prevalence -- it can also be about bias.
Shawn: One aspect is the number of people with that disability,
the other is the size of the body of research. We are trying to
balance it.
<Jan> Okay ... finally on
Shawn: it can also be under-representation in the research
Cybele: Using "prevalence" gives a context of number of people
in the disability. Shawn said it was more about
under-representation in the body of research.
Jan: I used prevalence is referencing small sample sizes
<JF> +1 to Jan
JF: We want to say that pure numbers will not influence final
decisions. Small groups have equally valid needs.
Shawn: It's more about the body of research
<KimD> Are we saying this? Be data-informed and evidence-based.
We recognize that research and evidence are influenced by both
the number of people with a particular disability and also by
the size of the body of research. The needs of the people with
disability shall be prioritized equally with all other groups.
<kirkwood> other than cognitive ;)
<Jan> +1 to KimD's wording
<Chuck> +1
<Lauriat> +1
<Makoto> +1 to KimD
<JF> +1
<kirkwood> +1
<KimD> Be data-informed and evidence-based. We recognize that
research and evidence are influenced by both the number of
people with a particular disability and also by the size of the
body of research. The needs of the people with disabilities
shall be prioritized equally with all other groups.
Are we saying this? Be data-informed and evidence-based. We
recognize that research and evidence are influenced by both the
number of people with a particular disability and also by the
size of the body of research. The needs of the people with
disabilities shall be prioritized equally with all other
groups.
<KimD> (fixed typo)
Racheal: We have people who fall under a large category of
disability but have individual needs.
<JF> We recognize that the amount of research and evidence
available are influenced by both the number of people with a
particular disability and also by the size of the body of
research.
<Cyborg> The intent is to make informed decisions wherever
possible and to ensure that the needs of all disability
categories are effectively represented. <--lost from Jan's
original wording
Jan: People with cognitive disabilities are the largest group
by size, but have individual needs and may not be covered by
the tools.
... people who are involved in standards work have noticed that
their group has not been well-represented and I'm not sure if
that is captured here.
<kirkwood> +1
Jan: In the COGA 2.1 work, the COGA group was asked "Where's
the research?" We need to rely on experts as well as research.
Bodies of experience and expertise
Rachel": Due to the complexities of some disability needs, we
will also rely on subject matter expertise.
<KimD> Is this better?
<KimD> Be data-informed and evidence-based. We recognize that
research and evidence are influenced by both the number of
people with a particular disability, by the size of the body of
research, and the difficulty in capturing research regarding
some disabilites. The needs of the people with disabilities
shall be prioritized equally with all other groups.
JF: In the absense of research, anecdotal evidence is
important, but it needs to be separate.
<ChrisLoiselle> I agree with JF, anecdotes would be rather soft
based evidence. Reliable research and actual data that provides
verifiable measurements / evidence.
Shawn: We need to be evidence-based where possible. In the
absense of hard data, we need to take anecdotal evidence.
Jan: We are creating a large loophole. We have struggled with
this on the COGA task force. We need to capture the
prepoderence of evidence in surveys and capturing experience of
individuals.
... we have to be careful of people influencing the standards
by manipulating the research.
Cybele: Can we encourage more research?
... I chafe with SME vs. experience of poeple with disabilities
JF: Lived experience is the weakest, because they have
individual experience.
... Subject matter expertise shows more than the individual
experience.
<kirkwood> volume evidence but specific application of evidence
to direct to requirements framework becomes somewhat difficult
Cybele: THere is something that chafes about that, my
experience in the last 10-15 years are that people with lived
experience have reached out in the community and actually have
real contextual exeriencee and insight.
<kirkwood> sorry, the volume evidence/research is great but
specific application of evidence to direct to requirements
framework becomes somewhat difficult
JF: We are dealing with two extremes and trying to find the
sweet spot in between.
Cybele: We need the word rigor. THe problem with research is
lack of rigor, the SME without empathy has a problem with
rigor, and the person with disabilities with too narrow a focus
lacks rigor.
<Cyborg> except i would spell it as rigour - lol (Canadian)
<ChrisLoiselle> If data-informed and evidence based, is within
the wording, I feel that we should note that it is objective
and observing what people do. SME's opinion would need to be
verified somehow , based on their own research to show proof of
evidence.
<Lauriat> +1 to Chris
JF: The example of WebAIM surveys is a good example of data
that may not have rigor because the audience isn't random, but
the body of resesarch from their surveys over time is valuable
and important.
<Cyborg> +1 to encouraging more research
<ChrisLoiselle> I.e. what is evidence?
Rachel: I propose another paragraph when we don't have evidence
what we will do.
<ChrisLoiselle> field visits, formative , summative usability
tests , a/b testing? task analysis? Those would be strong
evidence
Jan: I like that idea. I think we can set a procedure to handle
the circumstances where we don't have research.
Cybele: A lot of research is interpreted. We need to look at
the outliers as well as the conclusions.
<KimD> How about this:
<KimD> Be data-informed and evidence-based where possible. We
recognize that research and evidence are influenced by both the
number of people with a particular disability, by the size of
the body of research, and the difficulty in capturing data
regarding some disabilities. The needs of the people with
disabilities shall be prioritized equally with all other
groups.
<KimD> In situations where there is no evidence or research,
information may be obtained from advocacy groups, subject
matter experts and other others who can inform the design.
<Cyborg> my concern was about how evidence-based can equal
oppression of majority - and so interpretation of research
ought to address outliers' needs as well
<Cyborg> The intent is to make informed decisions wherever
possible and to ensure that the needs of all disability
categories are effectively represented. <--lost from Jan's
original wording
<Cyborg> +1 to John's change
<Lauriat> +1 to JF's change
+1 to JF's change
Be data-informed and evidence-based where possible. We
recognize that research and evidence are influenced by both the
number of people with a particular disability, by the size of
the body of research, and the difficulty in capturing data
regarding some disabilities. The needs of all people with
disabilities shall be prioritized equally. In situations where
there is no evidence or research,
information may be obtained from advocacy groups, subject
matter experts and other others who can inform the design.
<ChrisLoiselle> +1 to JF
<Makoto> +1 to JF
Be data-informed and evidence-based where possible. We
recognize that research and evidence are influenced by the
number of people with a particular disability, by the size of
the body of research, and the difficulty in capturing data
regarding some disabilities. The intent is to make informed
decisions wherever possible to ensure that needs of all people
with disabilities shall be prioritized
equally. In situations where there is no evidence or research,
information may be obtained from advocacy groups, subject
matter experts and other others who can inform the design.
<JF> +1
<Jan> Yay!! +1
<Cyborg> +1
<KimD> +1
<kirkwood> +1
<Cyborg> if i could +2 that would be good
<Lauriat> +1
<Chuck> +1
<JF> +1+1
<Makoto> +1, but what does it mean by "others who can inform
the design"?
+1
<Cyborg> we still need paragraph about encouraging research
that is rigorous, includes those at edges (not just address
needs of majority).
<Rachael> +1 but add some clarification about rigor and
aggregation on the last sentence
Jan: You may have a need and there may be others who have the
technical expertise.
JF: Technologists may not have subject matter experitise but
may have valuable expertise in how to implement the need.
Rachel: drop the "others"
<JF> In situations where there is no evidence or research,
information may be obtained from advocacy groups and subject
matter experts.
<kirkwood> +1 to JF but didn’t go in minutes
<Makoto> +1 to JF's edit.
<Jan> +1 to JF's recommendation
<Jan> We still need to add some additional text for rigor
Jan: We don't want to have people pointing to a blog post as
research. As that has happened in the past.
... I don't think we can use "rigor" but perhaps "methodical"?
<KimD> In situations where there is no evidence or research,
information may be obtained from advocacy groups, subject
matter experts, and other valid data- gathering methods.
<Cyborg> information-gathering and evaluation that aims to be
rigorous and includes those at the edges (rather than just
addressing the needs of the majority)
<ChrisLoiselle> valid and reliable data? i.e is it replicable?
<Rachael> Maybe: In situations where there is no evidence or
research, information may be obtained from a survey or other
methodical information gathering method of advocacy groups and
subject matter experts.
<Jan> In situations where there is no evidence or research,
valid data-gathering methods can be obtained from advocacy
groups, people with lived experience and other subject matter
experts.
<Rachael> In situations where there is no evidence or research,
valid data-gathering methods can be used to obtain information
from advocacy groups, people with lived experience and other
subject matter experts.
<Cyborg> +1 to Jan's wording
<Cyborg> or to Rachael's <- better
<KimD> +1, nice
<Jan> +1 to Rachael's
<Makoto> +1 to Rachael's wording
<JF> +1
<Chuck> +1
Be data-informed and evidence-based where possible. We
recognize that research and evidence are influenced by the
number of people with a particular disability, by the size of
the body of research, and the difficulty in capturing data
regarding some disabilities. The intent is to make informed
decisions wherever possible to ensure that needs of all people
with disabilities will be prioritized
equally. In situations where there is no evidence or research,
valid data-gathering methods can be used to obtain information
from advocacy groups, people with lived experience and other
subject matter experts.
+1
<Cyborg> outliers can be left out in research
<ChrisLoiselle> leaving meeting, thanks all.
<JF> Gotta drop - bye all
<Makoto> Arigato. Sayonara!
jeanne: LEt's take this up in email and resolve it before
Friday so we can get back to the WCAG to Silver Migration work.
Requirements: Technology Neutral
Jeanne notes that the agenda was incorrect (pasted from an
earlier email) and that the first topic was Technology Neutral.
I will fix it in the email but I can't fix the html minutes.
Summary of Action Items
Summary of Resolutions
1. [15]Guidance should be expressed in generic terms so that
they may apply to more than one platform or technology. The
intent of technology-neutral wording is to provide the
opportunity to apply the core guidelines to current and
emerging technology, even if specific technical advice
doesn't yet exist.
[End of minutes]
__________________________________________________________
Minutes manually created (not a transcript), formatted by
David Booth's [16]scribe.perl version 1.154 ([17]CVS log)
$Date: 2019/04/30 14:49:04 $
__________________________________________________________
Received on Tuesday, 30 April 2019 15:16:04 UTC