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Resistance Training as an Aid to Smoking Cessation Treatment

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01951456
Recruitment Status : Completed
First Posted : September 26, 2013
Last Update Posted : March 20, 2020
Sponsor:
Collaborator:
Brown University
Information provided by (Responsible Party):
Teachers College, Columbia University

Brief Summary:
The purpose of this study is to determine whether resistance training can aid smoking cessation.

Condition or disease Intervention/treatment Phase
Cigarette Smoking Behavioral: Resistance training Behavioral: Health and Wellness Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 180 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Resistance Training as an Aid to Smoking Cessation Treatment
Study Start Date : November 2013
Actual Primary Completion Date : March 31, 2019
Actual Study Completion Date : March 31, 2019

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Resistance training
Participants will attend two, 45-60-minute progressive, moderate intensity resistance training sessions per week for 12 weeks. The program will maintain a format of a 5-minute warm-up, 35-50 minutes of resistance training and a 5-minute cool-down with flexibility and abdominal exercises.
Behavioral: Resistance training
Active Comparator: Health and Wellness
Participants in this group will be required to attend the exact same number of sessions as those in the Resistance Training group. Each session will last approximately 45-60 minutes. Sessions will include a practical component/demonstration, an informational video, and a handout on a pertinent healthy lifestyle topic for adults.
Behavioral: Health and Wellness



Primary Outcome Measures :
  1. Smoking cessation [ Time Frame: Change from baseline to 3 months ]
    Salivary cotinine-verified 7-day Point Prevalence Abstinence (7-day PPA) from nicotine (cigarette smoking).


Secondary Outcome Measures :
  1. Cortisol [ Time Frame: 3, 6, 12 months ]
  2. Mood [ Time Frame: 3, 6, 12 months ]
  3. Cigarette cravings [ Time Frame: 3, 6, 12 months ]
  4. Abstinence self-efficacy [ Time Frame: 3, 6, 12 months ]
  5. Sleep [ Time Frame: 3, 6, 12 months ]
  6. Body composition [ Time Frame: 3, 6, 12 months ]
  7. Body weight [ Time Frame: 3, 6, 12 months ]
  8. Lung function [ Time Frame: 3, 6, 12 months ]
  9. Blood pressure [ Time Frame: 3, 6, 12 months ]
  10. Cholesterol profile [ Time Frame: 3, 6, 12 months ]
  11. Glycosylated hemoglobin [ Time Frame: 3, 6, 12 months ]
  12. Muscular strength [ Time Frame: 3, 6, 12 months ]
  13. Aerobic fitness [ Time Frame: 3, 6, 12 months ]
    Six-minute walk test

  14. Smoking cessation [ Time Frame: Change from baseline to 6 months ]
    Salivary cotinine-verified 7-day Point Prevalence Abstinence (7-day PPA) from nicotine (cigarette smoking).

  15. Smoking cessation [ Time Frame: Change from baseline to 12 months ]
    Salivary cotinine-verified 7-day Point Prevalence Abstinence (7-day PPA) from nicotine (cigarette smoking).



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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

Age 18 or older, smoke five or more cigarettes a day for at least the past 12 months

Exclusion Criteria:

Participating in any type of exercise for >60 minutes/week over the past 3 months, current smokeless tobacco use, participation in an ongoing effort to quit smoking, current or planned pregnancy, any serious medical condition that would make exercise unsafe


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01951456


Locations
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United States, New York
Teachers College, Columbia University
New York, New York, United States, 10027
Sponsors and Collaborators
Teachers College, Columbia University
Brown University

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Responsible Party: Teachers College, Columbia University
ClinicalTrials.gov Identifier: NCT01951456    
Other Study ID Numbers: 1R01HL117345-01A1 ( U.S. NIH Grant/Contract )
First Posted: September 26, 2013    Key Record Dates
Last Update Posted: March 20, 2020
Last Verified: April 2018
Keywords provided by Teachers College, Columbia University:
Smoking cessation
resistance training