Clinical Trials Directory

Trials / Completed

CompletedNCT01824511

Effects of Quitting Study A Test of Pre-clinical Findings

Does Smoking Cessation Increase Anhedonia? A Test of Pre-clinical Findings

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
287 (actual)
Sponsor
University of Vermont · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The most widely-accepted animal model of nicotine withdrawal states stopping nicotine makes rewarding events become less rewarding. The current study will test if this is true in humans. If we find tobacco abstinence does make rewards less rewarding, this would suggest new symptoms to add to official descriptions of nicotine withdrawal. It would also suggest we need to develop new behavioral and pharmacological interventions to correct this problem. If stopping smoking does not make rewards less rewarding, this would suggest this animal model does not apply to the human condition and we need to continue to search for an animal model of tobacco withdrawal that is relevant to smokers stopping smoking.

Detailed description

Study design We will recruit until we have 70 current smokers who want to quit at two sites (Univ of Vermont and Dartmouth Medical School). We will also recruit a comparison group of 70 long-time former smokers to assist in interpretation of the results. In the first week, smokers will smoke their usual number of cigs/day. They will then quit and are to remain abstinent for 4 weeks. We will use a schedule of escalating monetary contingencies based on breath and saliva and/or urine samples to encourage abstinence. We will obtain dependent measures twice/week. The primary measures of reward responsivity will be the percent choosing the hard task and the amount of responding for a monetary reward on the EEfRT task and the score on our Rewarding Events scale. Other outcomes will be delay discounting results and self-reports of anhedonia and apathy. The study will run for 1 week pre-cessation (2 visits) and then for 4 weeks post-cessation. Measures and biochemical verifications will occur twice/wk. Former smokers will attend once a wee for four weeks. For the first week of abstinence, the cutoff for nonsmoking will be CO \<8 ppm. For the remaining weeks, abstinence will be verified with a score of 0 (\<10 ng/ml of cotinine) on a test strip in a saliva or urine sample plus a CO \<8 ppm. At the initial session, completion of baseline surveys will describe the sample and also measure plausible moderators such as depression. We believe the most direct test of reward sensitivity is an evaluation of the influence of abstinence on operant responding for a reward. Thus, we have chosen performance on the Effort Expenditure for Rewards Task (EEfRT), which examines responding as a function of response cost, reward magnitude and probability of reward, as one of our primary outcomes. For a self-report measure we will use our Rewarding Events (RE) scale that asks both about occurrence of presumed rewarding events and their anticipated pleasantness. Our RE scale will ask participants to rate 58 items on frequency in the last week as well perceived/expected pleasantness of events. Secondary measures include the 18-item Apathy Evaluation Scale (AES), the Temporal Experience of Pleasure (TEPS), Minnesota Nicotine Withdrawal Scale-Revised (MNWS), and a measure of delay discounting (DD).

Conditions

Interventions

TypeNameDescription
BEHAVIORALSmokers cease smokingSmokers are paid to be abstinent for four weeks, and stop-smoking medications may not be used.

Timeline

Start date
2013-04-01
Primary completion
2015-09-01
Completion
2015-09-01
First posted
2013-04-04
Last updated
2016-03-14

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01824511. Inclusion in this directory is not an endorsement.