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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01501877
Other study ID # DA030532
Secondary ID
Status Completed
Phase N/A
First received December 21, 2011
Last updated April 10, 2017
Start date December 2011
Est. completion date June 2016

Study information

Verified date April 2017
Source Rhode Island Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to develop and test a smoking cessation intervention for smokers with Type 2 diabetes.


Description:

Individuals with Type 2 diabetes smoke at rates similar to those found in the general population, and the health consequences of smoking are particularly severe among smokers with diabetes. In fact, there appears to be a synergistic effect between smoking and diabetes on mortality. However, despite reports that highlight the importance of this work, a paucity of studies have been conducted to develop and test smoking cessation interventions tailored to meet the needs of individuals with diabetes. The small number of extant studies have yielded mixed results. Distress tolerance (DT) focused, acceptance-based interventions have demonstrated efficacy for smoking cessation, and there is increasing support for the conceptual model underlying these interventions among individuals with diabetes. The long-term objective of this research program is to improve smoking cessation treatment for individuals with Type 2 diabetes by developing and establishing the efficacy of a DT smoking cessation intervention tailored to this population. Furthermore, we seek to advance knowledge of the relationships among nicotine withdrawal, negative affect, distress tolerance, and smoking cessation outcomes among individuals with diabetes.

In the present study, we will develop a DT intervention tailored to meet the needs of smokers with Type 2 diabetes. In the first phase of this project, we will develop and pilot the intervention with 18 patients. In the second phase of the project, we will conduct a preliminary, randomized trial with 54 patients to examine the efficacy of the DT intervention relative to a standard smoking cessation treatment (ST) that equates for therapist contact time. Patients in both conditions will receive the transdermal nicotine patch.

We expect that, relative to the ST condition, patients randomized to the DT condition will have increased likelihood of smoking abstinence and increased latency to both smoking lapse and relapse. If the efficacy of this intervention can be established in this trial and in subsequent large scale randomized controlled trials, smokers with diabetes will have improved smoking cessation treatment options. The need for this work is great given the paucity of extant work in this area, the significantly heightened risk of morbidity and mortality from smoking among diabetic patients, the rapidly increasing rate of diabetes in the U.S., and an apparent stabilization of the smoking rate in recent years.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria:

- 21 years of age or older

- Type 2 diabetes

- regular smoker for at least 3 years

- smoke an average of more than 10 cigarettes per day

- report motivation to quit smoking of at least 5 out of 10

- speak English

Exclusion Criteria:

- current alcohol abuse or dependence

- current substance abuse or dependence (excluding nicotine)

- psychotic

- form of diabetes other than Type 2

- medical condition that is a contraindication for the transdermal nicotine patch

- using pharmacotherapy for smoking cessation

- using other tobacco products

- unable to provide names and contact information for locators

- no access to a telephone

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Acceptance and Commitment Therapy
The intervention is based on Acceptance and Commitment Therapy and will be tailored to smokers with Type 2 diabetes.
Standard smoking cessation intervention
Standard smoking cessation intervention based on clinical practice guidelines.

Locations

Country Name City State
United States Rhode Island Hospital Providence Rhode Island

Sponsors (1)

Lead Sponsor Collaborator
Rhode Island Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Point prevalence abstinence from smoking We will compare the percentage of participants in each treatment condition who report abstinence from smoking for the 7 days preceding the assessment. 26 weeks from smoking quit date
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