Actively Recruiting

Phase Not Applicable
Age: 15Years - 18Years
All Genders
ID07207850

Parents Helping Parents for Youth Vaping Cessation (PhP-VX)

Led by University of Nebraska · Updated on 2026-05-26

200

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

Sponsors

U

University of Nebraska

Lead Sponsor

M

Massachusetts General Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a new program called Parents-helping-Parents for Youth Vaping Cessation (PhP-VX) to help adolescents aged 15 to 18 quit vaping. This randomized controlled study aims to test if the program, which includes peer support for parents delivered by trained coaches, is feasible and helpful. The study will involve 100 parent-adolescent pairs recruited through an electronic health record system and will compare the program against no treatment control. The PhP-VX program has two main parts: online lessons for parents and adolescents, and six bi-weekly, 30-minute, one-on-one coaching sessions for parents via Zoom. Parents in the program will receive guidance on identifying needs, communication skills, motivation, and goal setting to support their teens. Parents can also contact coaches for extra support. The control group will receive no treatment during the 3-month intervention but will get access to online materials after the study ends. Participants will complete surveys at baseline, and at 1, 3, and 6 months to track vaping behavior, knowledge, and exposure to marketing. A subset of 20 adolescents may provide saliva samples at these time points to measure cotinine levels, a marker for nicotine exposure, to verify self-reported vaping abstinence. The primary outcome is 7-day vaping abstinence, with secondary outcomes including vaping frequency, intensity, and other tobacco use. The study lasts six months with continued follow-up for all participants.

CONDITIONS

Brief Title

Parents Helping Parents for Youth Vaping Cessation

Who Can Participate

Age: 15Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescents aged 15 to 18 years
  • Reported vaping in the previous 30 days
  • Able to read and understand English
  • Parent or adult guardian is biological, adoptive, stepparent, or legal guardian of the adolescent
  • Parent has face-to-face contact with the adolescent at least one day per week during the study
  • Parent has access to a computer or mobile phone at home
  • Parent is interested in helping the adolescent quit vaping
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person or remote)

Treatment

Duration - 3 months

Participants in the test group receive the PhP-VX program consisting of online lessons for parents and adolescents and six bi-weekly, 30-minute one-on-one coaching sessions for parents. Participants in the control group do not receive treatment during this period.

Six bi-weekly coaching sessions via Zoom for parents in the test group

Follow-up

Duration - 3 additional months following treatment

All participants complete surveys assessing vaping behavior, knowledge, and media literacy at months 1, 3, and 6. A subset of adolescent participants may provide saliva samples at baseline, 3 months, and 6 months for biochemical verification of tobacco abstinence.

Surveys at months 1, 3, and 6; saliva sample collection at baseline, 3, and 6 months for a subset

Trial Site Locations

Total: 1 location

1

University of Nebraska Medical Center

Omaha, Nebraska, United States, 68198-4375

Actively Recruiting

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Research Team

D

Daisy Dai, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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