Efficacy of Exercise and Counseling Intervention on Relapse in Smoker With Depressive Disorders (STOB-ACTIV)

University Hospital Center (CHU)

Status and phase: Terminated; Phase 3

Conditions: Depression; Smoking Cessation

Treatments: Behavioral: Exercise and counseling (for smoking cessation and physical activity)

Study type: Interventional

Funder types: Other

Identifiers

NCT01401569

8608

n°ID RCB 2010-A00119-30 (Other Identifier)

Details and patient eligibility

About

This study investigated the efficacy of an exercise and counseling intervention for depressed smokers (depression subscale of the Hospital Anxiety and Depression Scale, HADS-D score ≥ 8) in term of likelihood of smoking abstinence. Participants were randomized to 8 weeks of intervention: individually delivered exercise and counseling (for smoking cessation and physical activity) or control: health education contact control condition.

Full description

This study investigated the efficacy of an exercise and counseling intervention for depressed smokers (depression subscale of the Hospital Anxiety and Depression Scale, HADS-D score ≥ 8) in term of likelihood of smoking abstinence. Participants were randomized to 8 weeks of group delivered exercise and counseling (for smoking cessation and physical activity) or a health education contact control condition. The investigators assess this intervention in a randomized controlled trial of 96 depressed adults smokers recruited by advertisements in local print allocated into one of the two groups (intervention group vs. control group) during a 8-week period and 3 follow-up visits (12, 24, 52 weeks after baseline). All subjects (intervention and control groups) participate in a smoking cessation program composed of a pharmacological treatment (including nicotine replacement therapy or varenicline) and counseling.Experimental group subjects were required to attend 2 supervised exercise sessions and 2 counseling sessions during Week 1 and Week 2. Supervised exercise and counseling sessions are realized successively. For Week 3 to 8, participants were required to attend 1 supervised exercise session and 1 counseling session plus 1 home exercise session.Supervized exercise session consist of 5-min warm-up, 30 min of aerobic activity (stationary bikes), and a 5-min cooldown with stretching. The training intensity is of 60 to 80% maximum heart rate. The sessions are supervised by an exercise specialist who verified and documented the heart rates. Home exercise session consist of 45 min of aerobic exercise (walking, cycling, or running). The training intensity is 6 to 7 on breathlessness visual analog scale.The smoking counseling sessions included the following components: review of a participant's smoking history and motivation to quit, help in the identification of high-risk situations, management of cigarette craving and the generation of problem-solving strategies to deal with such situations.Exercise counseling sessions designed to motivate increased regular physical activity and short bouts of exercise in response to negative affect and urges to smoke. The goal of this intervention was to increase activity level.Health education group subjects were required to participate 75-minute supervised sessions with the same frequency of experimental group. Participants in the health education condition received information on a variety of health topics including sleep hygiene, nutrition, stress and health screening tests for cancer prevention. Participants were also asked to read handouts on health education topics covered during the session.

Enrollment: 70 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Ages 18 to 65 years
• Must be able to give informed consent
• Must live in the area for the next 3 months
• Depression subscale of the Hospital Anxiety and Depression Scale, HADS-D score ≥ 8
• Fagerstrom score > 3
• Must be sedentary, have not participated regularly in aerobic physical exercise (for at least 20 minutes per day, 3 days per week) for the past six months.
• Must be able to exercise at 60% maximum heart rate (MHR) (cleared by a physician)

Exclusion criteria

• Cannot read or write fluently in the French language
• Pregnancy or plans to attempt pregnancy
• 60 minutes or more per week of moderate or vigorous physical activity
• Currently in a quit smoking program
• Currently using NRT of any kind or using any other quit smoking method or treatment
• Poor willingness or inability to comply with protocol requirements

Medical problems:

• Cancer treatment within the past 6 monthsPsychiatric Problems
• Currently suicidal or psychotic, (or suicidal/psychotic in last 6 months)
• Taking these specific medications for psychiatric problems: Mood stabilizer (Lithium, Depakote, Neurontin), Antipsychotics (Haldol, Clozaril, Risperdal)
• Currently diagnosis of a bipolar disorder as assessed by MINI 5.0
• Currently diagnosis of a alcohol dependence as assessed by MINI 5.0

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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70 participants in 2 patient groups

Control

Active Comparator group

Description:

All subjects (intervention and control groups) participate in a smoking cessation program composed of a pharmacological treatment (including nicotine replacement therapy or varenicline) and counseling.

Treatment:

Behavioral: Exercise and counseling (for smoking cessation and physical activity)

physical activity program

Experimental group

Description:

Experimental group subjects were required to attend 2 supervised exercise sessions and 2 counseling sessions during Week 1 and Week 2. Supervised exercise and counseling sessions are realized successively. For Week 3 to 8, participants were required to attend 1 supervised exercise session and 1 counseling session plus 1 home exercise session.

Treatment:

Behavioral: Exercise and counseling (for smoking cessation and physical activity)