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Clinical Trials/NCT04928781
NCT04928781WithdrawnNot Applicable

Smoking Cessation Intervention for Hospitalized Heart & Vascular Center (HVC) Patients at a Dartmouth-Hitchcock Medical Center Serving a Rural Population

Dartmouth-Hitchcock Medical Center1 site in 1 countryStarted: June 28, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Locations
1
Primary Endpoint
Percentage of participants that self-report sustained smoking cessation

Study Overview

Brief Summary

This is a pilot study to determine the feasibility and success of offering smoking cessation counseling for ambulatory patients who present for scheduled cardiac catheterization.

Detailed Description

This is a prospective randomized pilot study of feasibility and success of smoking cessation counselling for ambulatory patients who present for scheduled cardiac catheterization. Patients who meet inclusion and exclusion criteria will be eligible for enrollment and receive smoking cessation counseling. Patients will be followed for 6 months post intervention. A Usual care arm will be created using retrospective chart review.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Presents to Dartmouth-Hitchcock Medical Center in Lebanon, NH as an ambulatory patient with a scheduled cardiac Catheterization
  • •smoke one or more cigarettes per day for the past 12 months OR use of electronic-cigarettes containing tobacco at least once during the past 30 days.
  • •proficient in English

Exclusion Criteria

  • Not provided

Arms & Interventions

Smoking Cessation Counseling - Intervention Arm

Experimental

Intervention arm. All patients enrolled in the study will be provided with smoking cessation counseling.

Intervention: Smoking Cessation Counseling (Behavioral)

Retrospective Chart Review - Control Arm

No Intervention

Control arm. A retrospective chart review will be conducted to create a randomly selected cohort of patients that meet inclusion and exclusion criteria and did not receive smoking cessation counseling to serve as the control arm.

Outcomes

Primary Outcomes

Percentage of participants that self-report sustained smoking cessation

Time Frame: 6 months post index procedure

Percentage of participants that self report sustained smoking cessation at 6 months.

Percentage of participants that self-report sustained smoking cessation

Time Frame: 1 month post index procedure

Percentage of participants that self report sustained smoking cessation at 1 month.

Percentage of participants that self-report sustained smoking cessation

Time Frame: 3 months post index procedure

Percentage of participants that self report sustained smoking cessation at 3 months.

Secondary Outcomes

  • Frequency of Cardiac Events following discharge from index procedure(6 months post index procedure)
  • Percentage of participants that need subsequent coronary intervention following index procedure(6 months post index procedure)
  • Percentage of participants that have had at least one subsequent cardiovascular hospital admission.(6 months post index procedure)
  • Percentage of participants that have had at least one emergency department presentation(6 months post index procedure)
  • Percentage of participants that have had at least one subsequent cardiovascular hospital admission.(1 month post index procedure)
  • Percentage of participants that have had at least one subsequent cardiovascular hospital admission.(3 months post index procedure)
  • Percentage of participants that have had at least one emergency department presentation(1 month post index procedure)
  • Percentage of participants that have had at least one emergency department presentation(3 months post index procedure)
  • Frequency of Cardiac Events following discharge from index procedure(1 month post index procedure)
  • Frequency of Cardiac Events following discharge from index procedure(3 months post index procedure)
  • Percentage of participants that need subsequent coronary intervention following index procedure(1 month post index procedure)
  • Percentage of participants that need subsequent coronary intervention following index procedure(3 moths post index procedure)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Merle L. Myerson

Staff Physician, Cardiovascular Medicine

Dartmouth-Hitchcock Medical Center

Study Sites (1)

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