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Tailored Web and Peer Email Cessation Counseling for College Smokers

RealU: Tailored Web and Peer Email Cessation Counseling for College Smokers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01604525
Acronym
RealU
Enrollment
1699
Registered
2012-05-23
Start date
2011-05-31
Completion date
2011-11-30
Last updated
2012-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cigarette Smoking

Brief summary

The RealU2 is a randomized controlled trial to determine the efficacy of an online health and wellness program for young adults with the addition of individualized peer health coaching.

Detailed description

The RealU addresses smoking in a young adult population of occasional and daily smokers. Aim 1. To determine the efficacy of providing individually tailored smoking cessation messages as part of a general interest website for young adults. Aim 2. To determine the efficacy of providing individually tailored smoking cessation messages plus peer email, phone and online support as part of a general interest website for young adults. Participants were recruited via direct emails sent to undergraduate and graduate students at the University of MI as well as direct emails sent to participants from Survey Sampling International and National Data Group. Individuals were invited to complete an online survey about health and hope in young adults. Participants eligible for the full intervention were invited to join the RealU Study. Participants were asked to complete an online enrollment survey and consent form. Eligible, enrolled participants were randomly assigned to one of the following three study arms: * an untailored general interest/lifestyle website * an individually tailored web intervention about health and lifestyle * an individually tailored web intervention about health and lifestyle with coaching from peers, including video, phone, and email Assessments were conducted at 7 weeks and 12 weeks post-enrollment. The primary outcome measure is self-reported 30-day abstinence at 12 weeks.

Interventions

BEHAVIORALTailored Web

The tailored website included 6 weeks of content about making healthy lifestyle choices, eating breakfast, exercising, reducing drinking and quitting smoking. Each week, participants were asked to check in with their past week's behavior, and to set goals for the next week's check-in.

BEHAVIORALPeer Coaching

Participants chose a peer coach, who reviewed the participant's check-in data and goals, and provided personalized feedback to help the participant reach those goals. Interaction took place via personalized videos recorded each week and uploaded to a participant's web profile, and through pro-active phone calls to the participants each week.

OTHERUntailored Web

Content about lifestyle issues (music, travel, dating) was created for participants assigned to the control group. There was new web content each week for 6 weeks.

Sponsors

National Heart, Lung, and Blood Institute (NHLBI)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-35 * Able to read English * Internet access for the next 3 months * Self-reported internet use of more than once per week * Smoked at least one puff of a cigarette in the past 30 days

Exclusion criteria

* Use of smokeless tobacco in the past 30 days

Design outcomes

Primary

MeasureTime frameDescription
Self-reported 30-day abstinence at Week 1212 weeks post-enrollmentParticipants were asked how many days they had smoked in the past 30 days during the follow-up survey conducted 12-13 weeks post-enrollment.

Secondary

MeasureTime frameDescription
Self reported 7-day abstinence at 7 weeks7-weeks post-enrollmentParticipants were asked to select which of the days in the past 7 (Sun-Sat) they had smoked even one puff.
Self-reported 7-day abstinence at Week 1212-weeks post-enrollmentParticipants were asked to select which days in the past 7 (Sun-Sat) they had smoked at least one puff.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026