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A Pilot Study Evaluating Nicotine Lozenges and Self Help

Watumiaji waliosajiliwa tu ndio wanaweza kutafsiri nakala
Ingia / Ingia
Kiungo kimehifadhiwa kwenye clipboard
HaliImekamilika
Wadhamini
Mayo Clinic
Washirika
Oregon Research Institute

Maneno muhimu

Kikemikali

The investigators are hypothesizing that by offering both self-help materials and mailed nicotine lozenges we will be able to help increase tobacco abstinence rates among ST users, as well as decrease tobacco withdrawal.

Maelezo

Smokeless tobacco (ST) is a known human carcinogen. Long-term ST use is known to increase the risk for oropharyngeal cancer. Most smokeless tobacco users wish to quit. Assisted-self help interventions (i.e., self-help manual, a targeted video, and two support telephone phone calls) have been shown to be superior to manual-only interventions for increasing tobacco abstinence rates. These interventions lend themselves to widespread dissemination, but abstinence rates at 6 months remains low (21%). Providing nicotine replacement therapy (NRT) to ST users receiving assisted self-help interventions could improve upon these ST abstinence rates. If found to be effective, this intervention may increase the ability to disseminate effective interventions to a population of tobacco users for whom few treatment resources currently exist.

Tarehe

Imethibitishwa Mwisho: 06/30/2011
Iliyowasilishwa Kwanza: 04/23/2009
Uandikishaji uliokadiriwa Uliwasilishwa: 04/23/2009
Iliyotumwa Kwanza: 04/26/2009
Sasisho la Mwisho Liliwasilishwa: 07/13/2011
Sasisho la Mwisho Lilichapishwa: 07/17/2011
Tarehe ya matokeo ya kwanza yaliyowasilishwa: 10/03/2010
Tarehe ya matokeo ya kwanza ya QC yaliyowasilishwa: 10/03/2010
Tarehe ya matokeo ya kwanza kuchapishwa: 11/03/2010
Tarehe halisi ya kuanza kwa masomo: 03/31/2008
Tarehe ya Kukamilisha Msingi iliyokadiriwa: 03/31/2009
Tarehe ya Kukamilisha Utafiti: 04/30/2009

Hali au ugonjwa

Smokeless Tobacco Use

Uingiliaji / matibabu

Drug: active

Drug: 2

Awamu

Awamu 2

Vikundi vya Arm

MkonoUingiliaji / matibabu
Active Comparator: active
Self-help counseling material and 4 mg nicotine lozenges
Drug: active
4 mg nicotine lozenges, ad lib, for 12 weeks.
Placebo Comparator: 2
self help counseling material and placebo nicotine lozenges
Drug: 2
Placebo nicotine lozenges

Vigezo vya Kustahiki

Zama zinazostahiki Kujifunza 18 Years Kwa 18 Years
Jinsia Inastahiki KujifunzaMale
Hupokea Wajitolea wa AfyaNdio
Vigezo

Inclusion Criteria:

1. male;

2. ≥18 years of age;

3. report ST as their primary tobacco of use;

4. have used ST daily for the past 6 months;

5. indicate that they want to quit;

6. have been provided with, understand, and have signed the informed consent.

Exclusion Criteria:

1. previously enrolled in a study involving the use of the nicotine lozenge;

2. currently using or have completed using (past 30 days) any other behavioral or pharmacologic tobacco treatment program;

3. currently enrolled in another research study;

4. describe having a medical history of: a) unstable angina; b) myocardial infarction within the past 6 months; c) cardiac dysrhythmia other than medication-controlled atrial fibrillation or PSVT; or d) medically-treated or untreated hypertension with BP ≥ 180 systolic OR ≥ 100 diastolic;

5. have phenylketonuria (PKU) [nicotine lozenges contain aspartame which is metabolized to phenylalanine and not processed in individuals with PKU];

6. have another member of their household already participating in this study;

7. have other medical or psychiatric conditions that would exclude the participant;

8. have a score of ≥ 15 on the Patient Health Questionnaire (PHQ-9) on the phone call pre-screen.

Matokeo

Hatua za Matokeo ya Msingi

1. Number of Participants With Tobacco Abstinence [12 weeks]

self-reported 7-day point prevalence tobacco abstinence at week 12 (end of treatment)

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