iPAWS: Helping teens manage pain and risky behaviors after wisdom tooth removal
Official title: iPAWS: Improving Pain Management After Wisdom Tooth Extraction Surgery
Run by Brown University · NCT07731295 · Data updated 2026-11-12
This program tests a short online intervention to help teens and their parents handle post-surgical pain and reduce risky behaviors after wisdom tooth extraction.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 15 Years to 20 Years |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | Brown University Academic / other |
| Locations | 1 site (Providence, Rhode Island) |
| Status | Recruiting |
| Started | June 29, 2026 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | July 28, 2026 |
| Trial ID | NCT07731295 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Teens and young adults aged 15–20 undergoing wisdom tooth extraction, who use cannabis at least two days per week, and their parent/guardian.
✕Probably not a fit
Individuals not using cannabis or who are outside the age range may not experience the same potential benefits.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial will assess the feasibility and acceptability of a virtual brief program for adolescents and young adults undergoing wisdom tooth extraction and their parents. It targets safe pain management and reductions in risky health behaviors, including cannabis use. The study will enroll participants aged 15 to 20 who are undergoing their first wisdom tooth extraction and meet cannabis-use criteria, delivering iPAWS educational materials as the intervention. Outcomes focus on user engagement, usability, and potential changes in pain coping strategies and health behaviors. The design is descriptive of feasibility, with Brown University and NIDA collaborating to support enrollment and data collection.
Why it matters
Potential benefit: If successful, participants may manage post-operative pain more effectively and reduce engagement in risky health behaviors during recovery.
How similar studies have gone: Prior virtual health education interventions have shown feasibility; this study applies a similar approach to post-surgical pain and behavior modification in a new age group and condition.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Ages 15 to 20 years * Undergoing wisdom tooth extraction for the first time * Able to read simple English * \*Endorse cannabis use at least two days per week on average in the past 28 days \*The investigator aims to recruit at least 50 participants who are using cannabis at least two days per week in the past 28 days on average and will recruit up to 100 additional participants who use other substances, use cannabis at a lesser intensity, or do not use any substances. * (Parent/Guardian only) - Have a child who is undergoing wisdom tooth surgery and is participating in the study Exclusion Criteria: \- N/A
Where it's running
-
Brown University Center for Alcohol and Addiction Studies
Providence, Rhode Island, United States Recruiting
Study contacts
- Study coordinator: Melissa Pielech, PhD
- Email: melissa_pielech@brown.edu
- Phone: 401-863-6583
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Low-Volume PENG Block With Dexamethasone After Hip Replacement
This trial tests whether a smaller PENG block with dexamethasone provides similar pain relief but preserves quadriceps strength after hip replacement, compared with the standard-volume PENG block.
-
Analgesia after open inguinal hernia repair using intrathecal morphine or a transversalis fascia plane block
This trial tests whether intrathecal morphine or a ultrasound-guided transversalis fascia plane block can provide better pain relief after open inguinal hernia repair in adults.
-
Single-level vs two-level erector spinae plane block for breast surgery
This study tests whether a single-level ESPB provides similar pain relief to a two-level ESPB for adults undergoing breast surgery.
-
Transverse vs Longitudinal Serratus Anterior Plane Block for Breast Surgery
This trial tests whether a longitudinal ultrasound view for serratus anterior plane block provides better pain relief after breast surgery than the standard transverse view.
-
Single-shot nerve block with IV dexamethasone for rebound pain after shoulder surgery
This trial tests whether giving a one-time shoulder nerve block plus an IV dexamethasone dose can prevent rebound pain after shoulder surgery.
-
Returning to the Land intervention for families in a tribal community
This program tests a biodiverse outdoor intervention with a tribal community to help reduce caregiver substance use and support emotional/behavioral development in children ages 1–5, by engaging families where teens 14–19 participate.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.