Evaluating a New Program for Successfully Coping With Adversity
NCT ID: NCT05354492
Last Updated: 2022-04-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
400 participants
INTERVENTIONAL
2021-02-01
2022-07-31
Brief Summary
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Detailed Description
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This study will take place remotely via phone and zoom. The initial interview/screening will take place via an online Qualtrics survey (follow-up by phone with the study coordinator), and the intervention sessions will be held online via Zoom with our trained intervention facilitators (licensed therapists). We will also be providing intervention support via a text messaging platform called Mobile Coach. The messages will be the same for all of the participants, and they will all receive them at the same time point in the program. All of the questionnaires will be completed online via a link that will be texted and/or emailed to the participant. Once participants see an advertisement and reach out to our study coordinator about their interest in the study, they will be directed to complete an online prescreening survey via Qualtrics to assess their eligibility for study participation. The study coordinator will then review the online survey and complete the cognitive screener and mental health questions by phone. If participants are eligible after the phone screen with the study coordinator, they will be scheduled to do a safety assessment via phone with one of our study clinicians. Once participants are deemed eligible, they will complete the consent form and be randomized into one of two conditions: active program or control. If a participant is randomized into the control condition, they will be placed on a "wait list" to receive the intervention at a later date. If a participant is randomized into the active program condition, they will be given the schedule for the group sessions, and sent a Zoom link for participation. The group intervention sessions will be guided by our trained facilitators for 75-90 minutes weekly for six weeks. After week 6, participants who were in the active program group will be asked complete a feedback form, as well as to take part in a semi-structured group interview to determine the acceptability and feasibility of the program. They will then enter the follow-up period of the study. Regardless of condition, participants will complete a set of questionnaires at Weeks 0, 3, 6, 9, and 12.
After week 12, participants who were randomized to the control condition will receive access to a recorded version of the intervention online. The recorded version will include the intervention developer talking through the intervention content and materials on video. No study participants will be included in this video.
This data will help to inform us whether the new improvements made to the SecondStory protocol are effective in improving participants' overall well-being and response to trauma, and will guide any future changes made to the intervention protocol.
Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Active Program Participant
You will actively take part in the group program via Zoom with our program facilitators.
Program to Support Well-Being after Adversity
You will be asked to meet on Zoom weekly for 6 weeks with our trained program facilitators along with the other 6-10 members of the intervention group. Meetings will last approximately 75-90 minutes each, and will involve a variety of discussions and activities related to navigating the changes you may face after experiencing a difficult life event. These sessions will be audio-recorded for research purposes and to ensure that facilitators are doing a good job delivering the program.
Program Wait List
You will be placed on a wait list to take part in the program.
No interventions assigned to this group
Interventions
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Program to Support Well-Being after Adversity
You will be asked to meet on Zoom weekly for 6 weeks with our trained program facilitators along with the other 6-10 members of the intervention group. Meetings will last approximately 75-90 minutes each, and will involve a variety of discussions and activities related to navigating the changes you may face after experiencing a difficult life event. These sessions will be audio-recorded for research purposes and to ensure that facilitators are doing a good job delivering the program.
Eligibility Criteria
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Inclusion Criteria
* Have experienced trauma within the last 3 months to 5 years
* Feeling some level of subjective distress as a result of the trauma
* Read and understand English
* Have consistent access to the internet
Exclusion Criteria
* Cognitive Impairment
* Diagnosed with a Psychotic Disorder
* Diagnosed with moderate to severe PTSD
18 Years
ALL
No
Sponsors
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John Templeton Foundation
OTHER
Wake Forest University
OTHER
Responsible Party
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Principal Investigators
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Eranda Jayawickreme, PhD
Role: PRINCIPAL_INVESTIGATOR
Wake Forest University
Locations
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Wake Forest University
Winston-Salem, North Carolina, United States
Countries
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Central Contacts
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Facility Contacts
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Casey Keller, MA
Role: primary
Other Identifiers
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IRB00024316
Identifier Type: -
Identifier Source: org_study_id