Purpose of Study
The purpose of this research study is to learn if a new online intervention program will help women feel better faster following a stressful event compared to the control group of participants. Participants will take surverys that will indicate if the treatment programs have been effective. The online intervention program is experiemental and has not been approved by the FDA.
Description of Study
This study utilizes online platforms to survey participants regarding experiences following stressful events to determine is online intervention program is effective.
Study Activities
| Activity | Value | Explanation |
| Initial onboarding | $20-40 | Surveys to determine eligibility, consent process if eligible |
| One week follow-up survey | $50 | Assesses current symptoms, allows them to opt in/out of wristband |
| Brief Surveys (weeks 0-7) | $1/ea Up to $196 | Brief surveys about how you’re feeling in that exact moment, or have for the day (asked to respond to at least 3/4 daily) |
| Wristband (weeks 1-7) | $2/day $5/wk bonus $25 return Up to $154 | Collects data about heart rate and skin conductance |
| Seven week follow-up survey | $50 | Assesses current symptoms and efficacy of treatment condition |
| 3.5 month check in | $10 | Confirms contact information is still up-to-date |
| Six month follow-up survey | $75 | Assesses remaining symptoms and efficacy of treatment condition |
