Stimulant Reduction Intervention using Dosed Exercise (STRIDE) - CTN 0037: Study protocol for a randomized controlled trial
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  • 作者:Madhukar H Trivedi (1)
    Tracy L Greer (1)
    Bruce D Grannemann (1)
    Timothy S Church (2)
    Eugene Somoza (3)
    Steven N Blair (4) (5)
    Jose Szapocznik (6)
    Mark Stoutenberg (6)
    Chad Rethorst (1)
    Diane Warden (1)
    Kolette M Ring (1)
    Robrina Walker (1)
    David W Morris (1)
    Andrzej S Kosinski (7)
    Tiffany Kyle (8)
    Bess Marcus (9)
    Becca Crowell (10)
    Neal Oden (11)
    Edward Nunes (12)
  • 关键词:stimulant abuse ; stimulant dependence ; exercise ; health education ; behavioral intervention
  • 刊名:Trials
  • 出版年:2011
  • 出版时间:December 2011
  • 年:2011
  • 卷:12
  • 期:1
  • 全文大小:419KB
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  • 作者单位:Madhukar H Trivedi (1)
    Tracy L Greer (1)
    Bruce D Grannemann (1)
    Timothy S Church (2)
    Eugene Somoza (3)
    Steven N Blair (4) (5)
    Jose Szapocznik (6)
    Mark Stoutenberg (6)
    Chad Rethorst (1)
    Diane Warden (1)
    Kolette M Ring (1)
    Robrina Walker (1)
    David W Morris (1)
    Andrzej S Kosinski (7)
    Tiffany Kyle (8)
    Bess Marcus (9)
    Becca Crowell (10)
    Neal Oden (11)
    Edward Nunes (12)

    1. The University of Texas Southwestern Medical Center at Dallas, 5323 Harry Hines Blvd, Dallas, Texas, 75390-9119, USA
    2. Preventive Medicine Laboratory, Pennington Biomedical Research Center, 6400 Perkins Rd, Baton Rouge, LA, 70808, USA
    3. Cincinnati Addictions Research Center (CinARC); Department of Psychiatry, University of Cincinnati College of Medicine, 260 Stetson St, Cincinnati, OH, 45219, USA
    4. Department of Exercise Science, University of South Carolina, 514 Main Street, Columbia, SC, 29208, USA
    5. Department of Epidemiology and Biostatistics, University of South Carolina, 800 Sumter Street, Columbia, SC, 29208, USA
    6. Department of Epidemiology and Public Health, University of Miami, Miller School of Medicine, 1120 NW 14th Street, Miami, 33136, FL, USA
    7. Department of Biostatistics and Bioinformatics, Duke University Medical Center, Duke Clinical Research Institute, P. O. Box 17969, Durham, NC, 27715, USA
    8. The Center for Drug-Free Living, 3670 Maguire Boulevard, Orlando, FL, 32853, USA
    9. Department of Family and Preventive Medicine, The University of California, San Diego, 9500 Gilman Drive, 0622, La Jolla, California, 92093-0622, USA
    10. Nexus Recovery Center, Inc, 8733 La Prada Dr, Dallas, Texas, 75228, USA
    11. The EMMES Corporation, 401 N. Washington St, Rockville, MD, 20850, USA
    12. New York State Psychiatric Institute/Department of Psychiatry, College of Physicians and Surgeons of Columbia University, 1051 Riverside Drive, Unit 69, New York, NY, 10032, USA
文摘
Background There is a need for novel approaches to the treatment of stimulant abuse and dependence. Clinical data examining the use of exercise as a treatment for the abuse of nicotine, alcohol, and other substances suggest that exercise may be a beneficial treatment for stimulant abuse, with direct effects on decreased use and craving. In addition, exercise has the potential to improve other health domains that may be adversely affected by stimulant use or its treatment, such as sleep disturbance, cognitive function, mood, weight gain, quality of life, and anhedonia, since it has been shown to improve many of these domains in a number of other clinical disorders. Furthermore, neurobiological evidence provides plausible mechanisms by which exercise could positively affect treatment outcomes. The current manuscript presents the rationale, design considerations, and study design of the National Institute on Drug Abuse (NIDA) Clinical Trials Network (CTN) CTN-0037 Stimulant Reduction Intervention using Dosed Exercise (STRIDE) study. Methods/Design STRIDE is a multisite randomized clinical trial that compares exercise to health education as potential treatments for stimulant abuse or dependence. This study will evaluate individuals diagnosed with stimulant abuse or dependence who are receiving treatment in a residential setting. Three hundred and thirty eligible and interested participants who provide informed consent will be randomized to one of two treatment arms: Vigorous Intensity High Dose Exercise Augmentation (DEI) or Health Education Intervention Augmentation (HEI). Both groups will receive TAU (i.e., usual care). The treatment arms are structured such that the quantity of visits is similar to allow for equivalent contact between groups. In both arms, participants will begin with supervised sessions 3 times per week during the 12-week acute phase of the study. Supervised sessions will be conducted as one-on-one (i.e., individual) sessions, although other participants may be exercising at the same time. Following the 12-week acute phase, participants will begin a 6-month continuation phase during which time they will attend one weekly supervised DEI or HEI session. Clinical Trials Registry ClinicalTrials.gov, NCT01141608 http://clinicaltrials.gov/ct2/show/NCT01141608?term=Stimulant+Reduction+Intervention+using+Dosed+Exercise&rank=1

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