iPAWS: Improving Pain Management After Wisdom Tooth Extraction Surgery
This study is testing a virtual program called iPAWS for young people aged 15 to 20 who are having their wisdom teeth removed for the first time. The iPAWS program combines different techniques to help manage pain and reduce risky health behaviors, especially for those who use cannabis. Participants will also receive educational materials from the American Dental Association. The main goals are to see if the iPAWS program is practical to deliver and if participants find it satisfactory. This study is looking for about 150 participants, including at least 50 who use cannabis at least two days a week.
- Study design
- This is an interventional study that plans to enroll about 150 participants. It is evaluating a behavioral intervention called iPAWS and educational materials.
- What's involved
- Participants will engage with the iPAWS behavioral intervention. They will also receive a digital brochure and can request a hard copy.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study measures outcomes at the end of the active treatment phase, which is 6 weeks.
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iPAWS: Improving Pain Management After Wisdom Tooth Extraction Surgery
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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Inclusion
What this trial measures
- Number of participants who complete the active treatment phase (feasibility)End of active treatment phase (6 weeks)
The number of participants who complete the active treatment phase will determine feasibility. The treatment will be considered feasible if the number of participants who complete treatment is ≥ 70%.
- Number of participants who rate their treatment experience in the "satisfactory" or "highly satisfactory" range on the Client Satisfaction Questionnaire (Acceptability)End of active treatment phase (6 weeks)
The Client Satisfaction Questionnaire (CSQ-8) which ranges in scores from 8 to 32 will determine acceptability. Higher scores indicate higher satisfaction (i.e. better outcomes). Treatment will be considered acceptable if the number and percentage of participants who rate their experience either "satisfactory" or "highly satisfactory is ≥ 80%.