Can a simple online program stop intimate partner violence? new study aims to find out.
NCT ID NCT07218159
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether an internet-based program called IDEA3, originally designed to prevent sexual assault, can also help prevent intimate partner violence (IPV) in undergraduate women. About 289 college women who already took part in a larger study will fill out one extra survey. Researchers will compare IPV rates between those who received the program and those who did not.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 289 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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May 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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17 to 26 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Enrolled in the IDEA3 parent study in September 2024 or later and completed the 12 month survey for the parent trial Original inclusion criteria for the parent trial: * 1st- and 2nd-year university students at one of the 4 sites * female-identifying students * students between ages of 17-24 at the time of enrollment into the parent trial * able to attend one of the scheduled program groups * able and willing to be matched with another eligible student Exclusion Criteria: * None
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
5 sites in 2 countries. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Central Florida
Orlando, Florida, 32816, United States
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University of Guelph
Guelph, Ontario, N1G 2W1, Canada
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University of Maryland
College Park, Maryland, 20742, United States
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University of Michigan
Ann Arbor, Michigan, 48109, United States
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University of Windsor
Windsor, Ontario, N9B 3P4, Canada
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