Comparative Effectiveness of Post-Discharge Strategies for Hospitalized Smokers (Helping HAND2)
Primary Purpose
Cigarette Smoking, Tobacco Smoking, Tobacco Use Disorder
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Sustained Care
Standard Care
Sponsored by
About this trial
This is an interventional treatment trial for Cigarette Smoking focused on measuring Cigarette smoking, Tobacco smoking, Tobacco use disorder
Eligibility Criteria
Inclusion Criteria:
- Cigarette smoker (smoked at least 1 cigarette in the month before hospital admission and at least 1 cigarette per day when smoking at baseline rate in the month before hospital admission)
- Counseled by hospital smoking counselor during hospital stay
- Plans to stop smoking tobacco products after hospital discharge
- Agrees to take home a supply of smoking cessation medication after discharge
- Agrees to and able to accept telephone calls after hospital discharge
Exclusion Criteria:
- No access to a telephone or unable to communicate by telephone
- Severe psychiatric or neurologic disease precluding ability to provide informed consent and to be counseled
- Pregnant, nursing, or planning to become pregnant in next 3 months
- Unable to speak English
- Medical instability precluding study participation
Sites / Locations
- Massachusetts General Hospital
- North Shore Medical Center
- University of Pittsburgh Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Experimental
Arm Label
Standard care
Sustained Care
Arm Description
At discharge, the participant receives the standard care provided by the hospital. This consists of a handout with information to contact the state telephone quitline for additional smoking cessation support and to use smoking cessation medication as recommended by the hospital smoking counselor.
A 3-month program after hospital discharge with these 2 components: (1) Free Medication and (2) Interactive Voice Response (IVR) Triage to Telephone Counseling.
Outcomes
Primary Outcome Measures
Tobacco Abstinence - 6 Month Follow-up
Cotinine-validated 7-day point prevalence tobacco abstinence at 6 month follow-up
Secondary Outcome Measures
Continuous Tobacco Abstinence
Continuous tobacco abstinence after hospital discharge assessed by self-report at 1, 3, and 6 months.
Point Prevalence Tobacco Abstinence
7-day point prevalence tobacco abstinence after hospital discharge, assessed by self-report
Duration of Tobacco Abstinence After Hospital Discharge
Self-reported number of days in which a participant was abstinent from tobacco after hospital discharge, by self-report, obtained from surveys done at 1 month, 3 months, and 6 months. Patient can only relapse once but it can occur at any point up to 6 months after discharge. Therefore, the data point can come from either the 1 or 3 or 6 month follow-up depending on when relapse occurred.
Use of Smoking Cessation Treatment After Hospital Discharge
Use of either FDA-approved pharmacotherapy for tobacco dependence (nicotine replacement therapy, bupropion, or varenicline), or psychosocial support (including telephone counseling, in person counseling, web-based counseling, physician counseling).
Full Information
NCT ID
NCT01714323
First Posted
October 22, 2012
Last Updated
May 11, 2018
Sponsor
Massachusetts General Hospital
Collaborators
University of Pittsburgh, North Shore Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01714323
Brief Title
Comparative Effectiveness of Post-Discharge Strategies for Hospitalized Smokers
Acronym
Helping HAND2
Official Title
Comparative Effectiveness of Post-Discharge Strategies for Hospitalized Smokers
Study Type
Interventional
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
December 2012 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
October 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
University of Pittsburgh, North Shore Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Cigarette smoking is the leading preventable cause of death in the U.S. The 2008 US Public Health Service Smoking Cessation Guideline recommends offering effective treatment to smokers in all health care settings, including hospitals. Nearly 4 million smokers are hospitalized each year, and hospital admission offers a "teachable moment" for intervention. Hospital-initiated smoking cessation intervention is effective, but only if contact continues for more than 1 month after discharge. The challenge is to translate this research into clinical practice by identifying an evidence-based cost-effective model that U.S. hospitals can adopt. The major barrier is sustaining contact after discharge. This project tests an innovative strategy to streamline the delivery and maximize the uptake of post-discharge smoking interventions.
Specific Aim: To test the effectiveness of an innovative strategy to maximize smokers' use of evidence-based tobacco treatment (counseling and medication) after hospital discharge, thereby increasing the proportion of smokers who achieve long-term (6-month) tobacco abstinence.
Study Design: A multi-site randomized controlled comparative effectiveness trial will enroll 1350 adult smokers admitted to 3 acute care hospitals in Massachusetts and Pennsylvania. All subjects will receive a brief in-hospital smoking intervention and be randomly assigned at discharge to either Standard Care (passive referral to their state quitline) or Extended Care, a 3-month program consisting of (1) Free Medication: A 30-day supply of FDA-approved medication (nicotine replacement, bupropion, or varenicline) given at hospital discharge and refillable for a total of 90 days to encourage medication use and adherence; (2) Interactive Voice Response (IVR) Triage to Telephone Counseling from a national quitline provider. IVR aims to encourage medication adherence and enhance counseling efficiency by identifying smokers who need post-discharge support. Immediate transfer of a patient from automated IVR call to live telephone counselor will facilitate a successful connection to counseling.
Outcomes, assessed at 1, 3, and 6 months after hospital discharge, are: (1) intervention effectiveness (cotinine-validated 7-day point-prevalence tobacco abstinence rate at 6 month follow-up [primary outcome] and other tobacco abstinence measures); (2) treatment utilization, and (3) cost-effectiveness (cost per quit). Exploratory analyses will examine the intervention's effect on hospital readmissions and mortality in the 6 months after discharge.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cigarette Smoking, Tobacco Smoking, Tobacco Use Disorder
Keywords
Cigarette smoking, Tobacco smoking, Tobacco use disorder
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1359 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard care
Arm Type
Other
Arm Description
At discharge, the participant receives the standard care provided by the hospital. This consists of a handout with information to contact the state telephone quitline for additional smoking cessation support and to use smoking cessation medication as recommended by the hospital smoking counselor.
Arm Title
Sustained Care
Arm Type
Experimental
Arm Description
A 3-month program after hospital discharge with these 2 components: (1) Free Medication and (2) Interactive Voice Response (IVR) Triage to Telephone Counseling.
Intervention Type
Behavioral
Intervention Name(s)
Sustained Care
Intervention Description
A 3-month program after hospital discharge with these 2 components: (1) Free Medication - A 30-day supply of FDA-approved medication (nicotine replacement, bupropion, or varenicline) given at hospital discharge and refillable for a total of 90 days to encourage medication use and adherence; (2) Interactive Voice Response (IVR) Triage to Telephone Counseling from a national quitline provider (Alere Wellbeing, Inc., previously Free & Clear). IVR aims to encourage medication adherence and enhance counseling efficiency by identifying smokers who need post-discharge support. Immediate transfer of a patient from automated IVR call to live telephone counselor will facilitate a successful connection to counseling.
Intervention Type
Behavioral
Intervention Name(s)
Standard Care
Intervention Description
Standard care consists of a handout with information about how to contact the state telephone quitline for additional smoking cessation support and to use smoking cessation medication as recommended by the hospital smoking counselor.
Primary Outcome Measure Information:
Title
Tobacco Abstinence - 6 Month Follow-up
Description
Cotinine-validated 7-day point prevalence tobacco abstinence at 6 month follow-up
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Continuous Tobacco Abstinence
Description
Continuous tobacco abstinence after hospital discharge assessed by self-report at 1, 3, and 6 months.
Time Frame
1 month, 3 months, 6 months
Title
Point Prevalence Tobacco Abstinence
Description
7-day point prevalence tobacco abstinence after hospital discharge, assessed by self-report
Time Frame
1 month, 3 months, 6 months
Title
Duration of Tobacco Abstinence After Hospital Discharge
Description
Self-reported number of days in which a participant was abstinent from tobacco after hospital discharge, by self-report, obtained from surveys done at 1 month, 3 months, and 6 months. Patient can only relapse once but it can occur at any point up to 6 months after discharge. Therefore, the data point can come from either the 1 or 3 or 6 month follow-up depending on when relapse occurred.
Time Frame
1 month, 3 months, 6 months
Title
Use of Smoking Cessation Treatment After Hospital Discharge
Description
Use of either FDA-approved pharmacotherapy for tobacco dependence (nicotine replacement therapy, bupropion, or varenicline), or psychosocial support (including telephone counseling, in person counseling, web-based counseling, physician counseling).
Time Frame
1 month, 3 months, 6 months
Other Pre-specified Outcome Measures:
Title
All-cause Hospitalizations
Description
Self-reported admission to a hospital in the 12 months after the index hospitalization.
Time Frame
12 months
Title
All-cause Mortality
Description
Death from any cause in the 6 months after hospital discharge
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Cigarette smoker (smoked at least 1 cigarette in the month before hospital admission and at least 1 cigarette per day when smoking at baseline rate in the month before hospital admission)
Counseled by hospital smoking counselor during hospital stay
Plans to stop smoking tobacco products after hospital discharge
Agrees to take home a supply of smoking cessation medication after discharge
Agrees to and able to accept telephone calls after hospital discharge
Exclusion Criteria:
No access to a telephone or unable to communicate by telephone
Severe psychiatric or neurologic disease precluding ability to provide informed consent and to be counseled
Pregnant, nursing, or planning to become pregnant in next 3 months
Unable to speak English
Medical instability precluding study participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nancy A Rigotti, MD
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Facility Name
North Shore Medical Center
City
Salem
State/Province
Massachusetts
ZIP/Postal Code
01970
Country
United States
Facility Name
University of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
31687769
Citation
Triant VA, Grossman E, Rigotti NA, Ramachandran R, Regan S, Sherman SE, Richter KP, Tindle HA, Harrington KF. Impact of Smoking Cessation Interventions Initiated During Hospitalization Among HIV-Infected Smokers. Nicotine Tob Res. 2020 Jun 12;22(7):1170-1177. doi: 10.1093/ntr/ntz168.
Results Reference
derived
PubMed Identifier
30156578
Citation
Streck JM, Chang Y, Tindle HA, Regan S, Park ER, Levy DE, Singer DE, Ylioja T, Rigotti NA. Smoking Cessation After Hospital Discharge: Factors Associated With Abstinence. J Hosp Med. 2018 Nov 1;13(11):774-778. doi: 10.12788/jhm.2997. Epub 2018 Aug 29.
Results Reference
derived
PubMed Identifier
29582077
Citation
Rigotti NA, Chang Y, Tindle HA, Kalkhoran SM, Levy DE, Regan S, Kelley JHK, Davis EM, Singer DE. Association of E-Cigarette Use With Smoking Cessation Among Smokers Who Plan to Quit After a Hospitalization: A Prospective Study. Ann Intern Med. 2018 May 1;168(9):613-620. doi: 10.7326/M17-2048. Epub 2018 Mar 27.
Results Reference
derived
PubMed Identifier
28616847
Citation
Rigotti NA, Chang Y, Rosenfeld LC, Japuntich SJ, Park ER, Tindle HA, Levy DE, Reid ZZ, Streck J, Gomperts T, Kelley JHK, Singer DE. Interactive Voice Response Calls to Promote Smoking Cessation after Hospital Discharge: Pooled Analysis of Two Randomized Clinical Trials. J Gen Intern Med. 2017 Sep;32(9):1005-1013. doi: 10.1007/s11606-017-4085-z. Epub 2017 Jun 14.
Results Reference
derived
PubMed Identifier
27647060
Citation
Rigotti NA, Tindle HA, Regan S, Levy DE, Chang Y, Carpenter KM, Park ER, Kelley JH, Streck JM, Reid ZZ, Ylioja T, Reyen M, Singer DE. A Post-Discharge Smoking-Cessation Intervention for Hospital Patients: Helping Hand 2 Randomized Clinical Trial. Am J Prev Med. 2016 Oct;51(4):597-608. doi: 10.1016/j.amepre.2016.04.005.
Results Reference
derived
PubMed Identifier
25879193
Citation
Reid ZZ, Regan S, Kelley JH, Streck JM, Ylioja T, Tindle HA, Chang Y, Levy DE, Park ER, Singer DE, Carpenter KM, Reyen M, Rigotti NA. Comparative Effectiveness of Post-Discharge Strategies for Hospitalized Smokers: study protocol for the Helping HAND 2 randomized controlled trial. BMC Public Health. 2015 Feb 7;15:109. doi: 10.1186/s12889-015-1484-0.
Results Reference
derived
Learn more about this trial
Comparative Effectiveness of Post-Discharge Strategies for Hospitalized Smokers
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