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Mobile Media-Rich Interactive Guideline System (MMRIGS) Pilot Study

Mobile Smoking Cessation Treatment for Underserved Smokers: A Pilot and Feasibility Study

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02302859
Enrollment
8
Registered
2014-11-27
Start date
2015-01-31
Completion date
2016-03-31
Last updated
2020-01-27

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

Conditions

Tobacco Use Cessation

Keywords

Cancer Prevention, Tobacco Use Cessation, HIV-positive, Nicotine patch, NRT, Questionnaire, Survey, Smartphone, Counseling, Saliva test, Saliva cotinine test, Nicotine replacement therapy, Smoking abstinence, Aids

Brief summary

The goal of this research study is to learn about 2 different interactive methods that are designed to help people with HIV/AIDS stop smoking.

Detailed description

Baseline Questionnaire: If you agree to take part in this study, you will complete a questionnaire on a laptop about your feelings, mood, health, thoughts about smoking, thoughts about quitting smoking, smoking history, and some demographic information such as age, education level, and income level. This should take about 15-20 minutes to complete. Study Groups: After completing the questionnaire, you will be randomly assigned (as in the flip of a coin) to 1 of 2 study groups. You will have an equal chance of being placed in either group. Both groups will receive smart phones and an 8-week supply of nicotine patches with instructions on how to use them. Each group will receive different methods of advice for quitting smoking. If you are assigned to Group 1, the following study procedures will be performed: * You will receive brief advice on how to quit smoking once at the time of enrollment. The advice will be given from a pamphlet that has information such as health problems related to smoking, how many Americans are affected each year, financial problems related to smoking, nicotine replacement therapy options, preparation for quitting smoking, and encouragement to quit. * On the smart phone, you will have 5 phone counseling sessions for support in quitting smoking throughout the 8-week intervention treatment. The calls should last about 15 minutes. If you are assigned to Group 2, the following study procedures will be performed: * On the smart phone, you will receive brief video clips with advice on how to quit smoking, as well as interactive text and picture messages once a week for 8 weeks. The video clips will be about 5 minutes long. * You will also have access to additional counseling content on the smart phone, which you can use at any time. Weekly Smart Phone Questionnaires: Both groups will complete questionnaires on the smart phone every week for 8 weeks. Each questionnaire will have questions about your current smoking status, your motivation level to stop smoking, and things that may have a negative effect on your quitting. The questionnaire should take about 15 minutes to complete. Follow-up Saliva Test and Questionnaire: About 3 months after your first smart phone intervention, both groups will complete a saliva test and take a photograph of the test results. The saliva test results will be used to check your smoking activity. Supplies and instructions will be given to you when you are enrolled on the study and the instructions will be available on the smart phone. You will also complete a questionnaire similar to the baseline questionnaire. Length of Study: You will be on study for about 3 months. This is an investigational study. Up to 50 participants will take part in this study. All will be enrolled at the Harris Health System (Thomas Street Health Center).

Interventions

DRUGNicotine Patch

Participants receive an 8 week supply of Nicotine patches.

BEHAVIORALQuestionnaires

Questionnaire completion at baseline on laptop, then weekly for 8 weeks on smartphone, then 3 months after smartphone intervention.

Pamphlet given to participant describing health and financial reasons to quit smoking.

BEHAVIORALPhone Counseling Sessions

Standard Treatment (ST) Group: Participants receive 8 phone counseling sessions (one session per week) for support in quitting smoking. The calls should last about 15 minutes. Automated Treatment (AT) Group: Participants receive brief video clips with advice on how to quit smoking over smartphone, as well as interactive text and picture messages once a week for 8 weeks. The video clips will be about 5 minutes long. Participants also have access to additional counseling content on the smart phone, which can be used at any time.

Participants complete saliva cotinine test 3 months after intervention.

Standard Treatment (ST) Group: Participants receive proactive phone counseling (8 sessions) over the 8-week period for support in quitting smoking. The call will last about 15 minutes. Automated Treatment (AT) Group: Participants receive brief advice to quit smoking (tailored video clips) and an 8-week automated intervention (interactive text messages and graphical messages) for support in quitting smoking via smartphone.

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. 18 years of age or older 2. Smoked at least 100 cigarettes in lifetime 3. English speaking 4. HIV-positive patient at Thomas Street Health Center 5. Currently smoking 5 or more cigarettes per day 6. Willing to make a quit attempt within 1 week of enrollment

Exclusion criteria

1. Positive history of a medical condition that precludes use of the nicotine patch 2. Current use of nicotine replacement therapy (NRT) 3. Current use of other smoking cessation medications (e.g., Chantix or Zyban) 4. Pregnant or nursing 5. Enrolled in another smoking cessation study

Design outcomes

Primary

MeasureTime frameDescription
Smoking Abstinence: 3-month Assessment Via Smart Phone3 monthsSmoking abstinence defined as number of participants with biochemically 7-day abstinence confirmed with weekly smart-phone assessments. Saliva cotinine levels, assessed with NicAlert test strips, used to biochemically verify abstinence. Participants will complete the NicAlert saliva cotinine test (supplies given at enrollment) and take a photograph of the test strip results. In primary abstinence analysis for difference in cessation rate between interventions, participants who do not complete follow-up assessments considered to be smokers.

Countries

United States

Participant flow

Recruitment details

Recruitment Period Opened January 2015 and Closed March 2016. Recruitment was accomplished in clinic setting of a large comprehensive HIV-care center.

Participants by arm

ArmCount
Standard Treatment (ST)
Participants receive 15-minute proactive weekly phone counseling sessions via smartphone along with supply of nicotine patches for 8-week period to support quitting smoking.
2
Automated Treatment (AT)
Participants receive brief weekly advice (tailored 5 minute video clips) and 8-week automated intervention (interactive text messages and graphical messages via smartphone) along with supply of nicotine patches for 8-week period to support quitting smoking.
6
Total8

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost Phone11
Overall StudyWithdrawal by Subject01

Baseline characteristics

CharacteristicStandard Treatment (ST)Automated Treatment (AT)Total
Age, Continuous46 years54 years51 years
Region of Enrollment
United States
2 participants6 participants8 participants
Sex: Female, Male
Female
2 Participants2 Participants4 Participants
Sex: Female, Male
Male
0 Participants4 Participants4 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 20 / 6
other
Total, other adverse events
0 / 20 / 6
serious
Total, serious adverse events
0 / 20 / 6

Outcome results

Primary

Smoking Abstinence: 3-month Assessment Via Smart Phone

Smoking abstinence defined as number of participants with biochemically 7-day abstinence confirmed with weekly smart-phone assessments. Saliva cotinine levels, assessed with NicAlert test strips, used to biochemically verify abstinence. Participants will complete the NicAlert saliva cotinine test (supplies given at enrollment) and take a photograph of the test strip results. In primary abstinence analysis for difference in cessation rate between interventions, participants who do not complete follow-up assessments considered to be smokers.

Time frame: 3 months

Population: Data were not collected due to early termination of the protocol

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