The SMOKE Telehealth Study

Part of paid clinical trials in Binghamton, New York.

Sponsor
Binghamton University
Study ID
NCT07743710
Status
Recruiting
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Conditions

  • Tobacco Smoking

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Smoking and Health Telehealth Intervention 1 — BEHAVIORAL
    The Smoking and Health Telehealth Intervention 1 provides educational information about how smoking is related to health and resources for smoking cessation. The intervention is delivered via live telehealth online in a single (30 minute) session.
  • Smoking and Health Telehealth Intervention 2 — BEHAVIORAL
    The Smoking and Health Telehealth Intervention 2 provides educational information about how smoking is related to health and resources for smoking cessation. The intervention is delivered via live telehealth online in a single (30 minute) session.

Study Details

The goal of this clinical trial is to develop two health-focused interventions for tobacco smokers with chronic pain. The main questions it aims to answer are: * Are the interventions feasible for delivery via telehealth? * Are the interventions acceptable to participants? This study has two phases. First, researchers will develop materials and receive feedback through three focus groups, updating the materials iteratively between each group. Next, researchers will compare the feasibility and acceptability of the two interventions. Participants in the second phase will: * Complete the a single-session telehealth intervention online * Complete surveys online before, immediately after, and at 2-weeks, 1-month, and 3-months after the intervention session.

Key Dates

First listed
Aug 4, 2026
Start date
Dec 19, 2025
Status verified
Jul 2026
Primary completion
Jul 31, 2027
Completion
Jul 31, 2027

Study Design

Enrollment
78 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Smoking and Health Intervention 1
  • Experimental: Smoking and Health Intervention 2

Primary Outcome Measure

Recruitment Feasibility [ Time Frame: At the participant level, time from screening through enrollment is anticipated to be up to 4 weeks. The total will be calculated at the end of the entire enrollment period of the study, which is anticipated to be approximately 1 year and 9 months. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Binghamton UniversityBinghamtonNew York13905
Emily Zale
[email protected]
7196507236
Emily Zale (PRINCIPAL_INVESTIGATOR)

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