Anna M Polaski1,2, Amy L Phelps2,3, Thomas J Smith4, Eric R Helm5, Natalia E Morone6, Kimberly A Szucs2,7, Matthew C Kostek2,8, Benedict J Kolber1,2,9. 1. Department of Biological Sciences, Duquesne University, Pittsburgh, Pennsylvania, USA. 2. Chronic Pain Research Consortium, Duquesne University, Pittsburgh, Pennsylvania, USA. 3. Palumbo-Donahue School of Business, Duquesne University, Pittsburgh, Pennsylvania, USA. 4. Counseling and Wellbeing Center, Duquesne University, Pittsburgh, Pennsylvania, USA. 5. Department of Physical Medicine and Rehabilitation, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA. 6. Section of General Internal Medicine, Boston University School of Medicine, Boston Medical Center, Boston, Massachusetts, USA. 7. Department of Occupational Therapy, Duquesne University, Pittsburgh, Pennsylvania, USA. 8. Department of Physical Therapy, Duquesne University, Pittsburgh, Pennsylvania, USA. 9. Department of Neuroscience and Center for Advanced Pain Studies, University of Texas at Dallas, Richardson, Texas, USA.
Abstract
OBJECTIVE: This pilot trial examined the effects of a combined intervention of mindfulness meditation followed by aerobic walking exercise compared with a control condition in chronic low back pain patients. We hypothesized that meditation before exercise would reduce disability, pain, and anxiety by increasing mindfulness prior to physical activity compared with an audiobook control group. PARTICIPANTS: Thirty-eight adults completed either meditation and exercise treatment (MedExT) (n=18) or an audiobook control condition (n=20). SETTING: Duquesne University Exercise Physiology Laboratory. DESIGN: A pilot, assessor-blinded, randomized controlled trial. METHODS: Over a 4-week period, participants in the MedExT group performed 12-17 minutes of guided meditation followed by 30 minutes of moderate-intensity walking exercise 5 days per week. Measures of disability, pain, mindfulness, and anxiety were taken at baseline and postintervention. Pain perception measurements were taken daily. RESULTS: Compared with the control group, we observed larger improvements in disability in the MedExT intervention, although the changes were modest and not statistically significant (mean between-group difference, -1.24; 95% confidence interval [CI], -3.1 to 0.6). For secondary outcome measures, MedExT increased mindfulness (within-group) from pre-intervention to postintervention (P=0.0141). Additionally, mean ratings of low back pain intensity and unpleasantness significantly improved with time for the MedExT group compared with that of the control group, respectively (intensity P=0.0008; unpleasantness P=0.0022). CONCLUSION: . Overall, 4 weeks of MedExT produced suggestive between-group trends for disability, significant between-group differences for measures of pain, and significant within-group increases in mindfulness.
OBJECTIVE: This pilot trial examined the effects of a combined intervention of mindfulness meditation followed by aerobic walking exercise compared with a control condition in chronic low back pain patients. We hypothesized that meditation before exercise would reduce disability, pain, and anxiety by increasing mindfulness prior to physical activity compared with an audiobook control group. PARTICIPANTS: Thirty-eight adults completed either meditation and exercise treatment (MedExT) (n=18) or an audiobook control condition (n=20). SETTING: Duquesne University Exercise Physiology Laboratory. DESIGN: A pilot, assessor-blinded, randomized controlled trial. METHODS: Over a 4-week period, participants in the MedExT group performed 12-17 minutes of guided meditation followed by 30 minutes of moderate-intensity walking exercise 5 days per week. Measures of disability, pain, mindfulness, and anxiety were taken at baseline and postintervention. Pain perception measurements were taken daily. RESULTS: Compared with the control group, we observed larger improvements in disability in the MedExT intervention, although the changes were modest and not statistically significant (mean between-group difference, -1.24; 95% confidence interval [CI], -3.1 to 0.6). For secondary outcome measures, MedExT increased mindfulness (within-group) from pre-intervention to postintervention (P=0.0141). Additionally, mean ratings of low back pain intensity and unpleasantness significantly improved with time for the MedExT group compared with that of the control group, respectively (intensity P=0.0008; unpleasantness P=0.0022). CONCLUSION: . Overall, 4 weeks of MedExT produced suggestive between-group trends for disability, significant between-group differences for measures of pain, and significant within-group increases in mindfulness.
Authors: Tonya L Jacobs; Phillip R Shaver; Elissa S Epel; Anthony P Zanesco; Stephen R Aichele; David A Bridwell; Erika L Rosenberg; Brandon G King; Katherine A Maclean; Baljinder K Sahdra; Margaret E Kemeny; Emilio Ferrer; B Alan Wallace; Clifford D Saron Journal: Health Psychol Date: 2013-03-25 Impact factor: 4.267
Authors: Stefan Schmidt; Sophia Gmeiner; Claudia Schultz; Marc Löwer; Klaus Kuhn; José Raúl Naranjo; Christina Brenneisen; Thilo Hinterberger Journal: Forsch Komplementmed Date: 2015-10-16