跳至主要内容
临床试验/NCT02607514
NCT02607514已完成不适用

Mechanisms of Hyperthermic Yoga for the Treatment of Depression

Massachusetts General Hospital2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2017年2月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
2
主要终点
Acceptability as Measured by the Acceptability Interview Completed at 8-week Endpoint or Early Termination

研究概览

简要总结

Study is a randomized controlled trial to assess the feasibility, acceptability, efficacy, and mechanisms of action of hyperthermic yoga versus a waitlist control for 80 medically healthy adults with mild to moderate depressive symptoms. The primary aim is to test the acceptability and feasibility of hyperthermic yoga as a treatment for depression. The secondary aim is to examine the effect size/efficacy of hyperthermic yoga for depressive symptoms. The tertiary aim is to explore physiological and psychological mechanisms of action.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adults ages 18-60
  • English language proficiency
  • Ability to provide informed consent
  • Score of >23 on the Inventory of Depressive Symptomatology - Clinician Rated (IDS-CR)
  • Able and willing to attend two 90-minute hyperthermic yoga sessions per week
  • Willingness to keep existing exercise regimen (even if that is sedentary) stable over study course
  • Women of childbearing potential must use an acceptable form of birth control
  • Membership to the Bikram Yoga Boston and Bikram Yoga Cambridge studios via studio website "Interested in research" option through a centralized portal (this will remain central until January 1, 2017)
  • Willingness to adhere to hydration requirements (i.e., an additional four 8 oz servings of water pre- and post-yoga classes)

排除标准

  • Pregnancy or planned pregnancy during study
  • History of psychiatric hospitalization within the past year
  • Active suicidal intent within the past year ("yes" on item 4 or 5 on the Columbia-Suicide Severity Rating Scale)
  • History of neurologic disorders that could interfere in study participation
  • History of bipolar disorder, psychotic disorders, eating disorders, and/or substance abuse or dependence (within the last year), as per the Mini-International Neuropsychiatric Interview (MINI)
  • Psychotropic medication use that has been stable for <3 months
  • Use of stimulant medications or diet pills during the study, or any pre-workout powders or liquids designed to provide excessive energy
  • Positive urine toxicology screen due to illicit drug use or other exclusionary medications. (Potential false positives will be addressed on a case-by-case basis at the discretion of the investigator)
  • Active conditions which may also cause depressive symptoms (e.g. epilepsy, hypothyroidism)
  • Medical conditions that may make participation unsafe (e.g., diabetes [I & II], cardiovascular disease, hypertension [>140 systolic and/or >90 diastolic], hypotension [<90 systolic and/or <60 diastolic, during screening], orthostatic hypotension [systolic drop of 20 points or 10 point diastolic or heart rate increase by 10], autoimmune disorders, malignancy, or autonomic dysfunction)
  • > 6 one hour classes of meditation or other mind-body disciplines (e.g., Tai chi or yoga) within the last 6 months
  • Current individual or group psychotherapy established for <3 months
  • A subject who in the opinion of the Principal Investigator would not be able to safely complete the study or would jeopardize study integrity
  • History of heat intolerance or heat stroke
  • Unsafe cardiac status as defined by abnormal ECG reading at screening visit as determined by medical monitor, study doctor, or subject's PCP or cardiologist

研究组 & 干预措施

immediate yoga arm

Experimental

participants will immediately start the 8-week hyperthermic yoga intervention

干预措施: hyperthermic yoga (Behavioral)

delayed yoga arm

Other

participants will wait 8-weeks to start the 8-week hyperthermic yoga intervention

干预措施: hyperthermic yoga (Behavioral)

结局指标

主要结局

Acceptability as Measured by the Acceptability Interview Completed at 8-week Endpoint or Early Termination

时间窗: at the end of 8-weeks or early termination.

Acceptability Interview: A 19-question qualitative interview assesses perception of ease of participation, program likeability, and perceived benefits of the yoga program. Adapted from DeBoer et al. It was a 1-10 likert scale with 1 = lowest, 10 = highest to rate acceptability of the yoga intervention. These are the items we used: 1) how much did you enjoy the yoga itself?; 2) how much did you enjoy the aftereffects of the yoga?; and 3) how reasonable did you find the time commitment to be?

Feasibility and Tolerability Measured by Percent of the Yoga Group Who Complete a Week 8 Assessment

时间窗: 8-week primary end point

Measured by percent of the yoga group who complete a week 8 assessment

Depressive Symptoms as Measured by the Inventory of Depressive Symptomatology - Clinician Rated (IDS-CR)

时间窗: 8-week primary endpoint

Inventory of Depressive Symptomatology - Clinician Rated. Scale range: 0-84 (higher = greater depressive symptoms)

次要结局

  • Anxiety as Measured by the Spielberger State-Trait Anxiety Inventory (STAI), Trait, Over 8 Weeks.(8 weeks)
  • Long Term Effects of Heated Yoga Intervention as Measured by All Primary and Secondary Outcomes After 1 Month Post-intervention.(one month post intervention)
  • Anxiety as Measured by the Spielberger State-Trait Anxiety Inventory (STAI), State, Over 8 Weeks.(8 weeks)
  • Sleep as Measured by the Pittsburg Sleep Quality Index (PSQI): A Commonly Used and Well-validated Self-rated Measure of Sleep-quality and Disturbance Over 8-weeks.(8-weeks)
  • Quality of Life as Measured by the Quality of Life Satisfaction Questionnaire-Short Form (Q-LES-Q-SF) Over 8 Weeks.(8-weeks end point)
  • General Health as Measured by the Medical Outcomes Study 36-item Short-form Survey (SF-36)(8 weeks)
  • Physical Functioning as Measured by the Physical Component Scale (PCS) of the Medical Outcomes Study 36-item Short-form Survey (SF-36) Over 8 Weeks.(8 weeks)
  • Perceived Stress as Measured by the Perceived Stress Scale (PSS) Over 8 Weeks.(8 weeks)
  • Long Term Effects of Heated Yoga Intervention -- IDS-CR(one month post intervention)
  • Long Term Effects of Heated Yoga Intervention -- PSQI(baseline to 1-month follow-up)
  • Long Term Effects of Heated Yoga Intervention -- QLESQ(baseline to 1-month follow-up)
  • Long Term Effects of Heated Yoga Intervention -- SF-36 PF(baseline to 1-month follow-up)
  • Long Term Effects of Heated Yoga Intervention -- SF-36 GH(baseline to 1-month follow-up)
  • Long Term Effects of Heated Yoga Intervention -- PSS(baseline to 1-month follow-up)
  • Long Term Effects of Heated Yoga Intervention -- STAI State(baseline to 1-month follow-up)
  • Long Term Effects of Heated Yoga Intervention -- STAI Trait(baseline to 1-month follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Maren Nyer

Maren Nyer, PhD

Massachusetts General Hospital

研究点 (2)

Loading locations...

相似试验