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Addressing Tobacco Use Disparities in Rural Older Adults Through an Innovative Mobile Phone Intervention

Addressing Tobacco Use Disparities in Rural Older Adults Through an Innovative Mobile Phone Intervention: Testing the Feasibility of the Textto4gotobacco Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02510716
Enrollment
40
Registered
2015-07-29
Start date
2015-12-31
Completion date
2016-09-30
Last updated
2016-10-21

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

Conditions

Tobacco Cessation

Brief summary

The purpose of this study is to evaluate the feasibility, acceptability and preliminary efficacy of a Scheduled Gradual Reduction (SGR) intervention via SMS (short message service) text messaging plus SMS Support Messages in decreasing smoking in an older adult rural population. The SGR group (n=20) will receive a four-week SGR program delivered via SMS text messages plus SMS support messages. The control group (n=20) will receive SMS support messages to aid in quitting.

Interventions

BEHAVIORALSGR
BEHAVIORALSupport message only

Sponsors

Mayo Clinic
CollaboratorOTHER
Alliance for Clinical Trials in Oncology
CollaboratorOTHER
Duke Cancer Institute
CollaboratorOTHER
Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

1. Over 60 years of age, 2. Have smoked 100 cigarettes in their lifetime and currently smoke five or more cigarettes a day on average, 3. Have an address in a rural census tract defined by a RUCA code of 4-10, 4. Interested in participating in a cessation program, 5. Own a phone that has texting ability and free texting, 6. Have general knowledge of text messaging and 7. Are willing to receive and respond to text messages from the study teams, throughout the duration of the study.

Exclusion criteria

1. criteria include non-English speaking patients 2. already participating in a smoking cessation intervention study.

Design outcomes

Primary

MeasureTime frameDescription
Tobacco cessation, defined as quit rate at 30 days, as measured by self-reported abstinence from tobacco use30-daysQuit rate at 30 days, as measured by self-reported abstinence from tobacco use

Secondary

MeasureTime frameDescription
Feasibility, as measured by proportion of return text messages30 daysProportion of return text messages sent per participants upon receiving alert text messages to use tobacco in the intervention group at 30 days Proportion of SMS support messages opened and/or read per participant
Acceptability, as measured by percentage of participants who reported that they would recommend the program to a friend30 daysPercentage of participants who reported that they would recommend the program to a friend

Countries

United States

Outcome results

None listed

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