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Participants have to be:
1) 18 years or older 2) married or living common-law for at
least 1 year
Purpose and Design
The purpose of this survey is to investigate
the role of spirituality (e.g., relationship with God
or higher power) in coping with stress that you are
currently experiencing in your relationship with a significant
other or partner. We are interested in the following
two groups of participants for this study: 1) individuals
with a history of childhood sexual abuse and 2) individuals
who do not have a history of childhood abuse.

Study Prodedures
This is a questionnaire study that you can complete
in the comfort of your own home on this website. There
are 11 inventories which ask about: demographic factors
(e.g., age), the nature of your childhood sexual abuse
(if applicable), how you cope with current interpersonal
stress, personal attitudes, spirituality, forgiveness,
social support, emotional well-being and your sense
of satisfaction in your partner relationship. The website
is designed so that when you finish one inventory and
continue to the next, your responses are submitted directly
to the database server. Please note that you can skip
any questions that you do not feel comfortable answering.

Length of Study
Your participation in this study will take anywhere
from 30-60 minutes depending on how quickly you move
through the material.
Possible Risks
Since the questionnaires do involve items of
a personal nature about how you are feeling and coping
with current life event stress as well as your past
abuse (if applicable) minimal emotional discomfort may
occur. If you experience any discomfort or have any
inquiries about the questionnaires, do not hesitate
to contact the principal investigator, Dr. Terry Lynn
Gall (tgall@ustpaul.ca).
If you so request and live in the Ottawa region, Dr.
Gall can provide you with a list of counseling services
or other services in the community. Remember, you do
not have to complete this questionnaire.

Benefits of the Study
Although you may not receive direct benefit
from participation in this study, you will be providing
information that could help in the future development
of counseling interventions for adult survivors of childhood
sexual abuse.

Confidentiality
To ensure anonymity we will provide you with
a unique identifier which will protect your identity.
This identifier will allow us to match up your inventories
as they are submitted. We ask that you do not enter
your name on the questionnaire. The data submitted to
the database server by you will not include any information
that can be used to identify you including the IP (internet
protocol) address of your computer. To ensure confidentiality,
the data on the server can only be accessed by an encrypted
code known by the researchers. All data will eventually
be downloaded in files and stored in a locked area at
Saint Paul University. To comply with ethics regulations,
this data has to be stored for a period of five years
after the publication of the study results after which
it will be appropriately destroyed. Data will be reported
as group results in any publications or presentations
and so your personal information will not be identifiable.

Voluntary Participation
Your participation in this study is completely
voluntary. You are under no obligation to participate
in this study and you can choose not to participate
by exiting the website at any time. Any partial data
that is collected will be destroyed.

Questions about the Study
This research is being conducted by Dr. Terry
Lynn Gall, associate professor in the Faculty of Human
Sciences, Saint Paul University, Ottawa, Ontario, Canada
(613-236-1393 x.2279). The principal investigator, Dr.
Gall can be reached at her email address: tgall@ustpaul.ca
if you have any questions and/or concerns about this
study. If you have any questions about your rights as
a research participant, you can contact Ming Zhang,
Director of Research Services, Saint Paul University
at: mzhang@ustpaul.ca.

Consent
The completion and submission of this web-based
questionnaire will indicate your full consent to participate
in this study.

Thank You for your
participation
Click here to begin.
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