- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04288830
Evaluation of a Tai Chi Resilience Training Program on Objective and Subjective Measures of Post Traumatic Stress Disorder Severity
Study Overview
Status
Intervention / Treatment
Detailed Description
Post-traumatic stress disorder (PTSD) affects an estimated 4.7% of the United States population every year, leading to increased rates of disability, suicide, substance use, and interpersonal difficulties. Mindfulness interventions for PTSD offer a low-cost, repeatable method that has the potential to induce fear extinction, and that has no known side effects. While several studies have reported the efficacy of mindfulness meditation and related mind-body exercises to reduce self-reported PTSD symptoms, little is known about the physiologic changes associated with mindfulness interventions. The present study seeks to evaluate the effects of a mind-body mindfulness intervention (tai chi) on subjective reports of PTSD symptoms, as well as physiologic correlates of PTSD in a population of law enforcement officers. Tai chi was chosen because its focus on awareness of physical movements is expected to provide an easier mindfulness target, as compared to traditional seated meditation. It is well documented that patients with PTSD, who frequently struggle with intrusive trauma-related memories, are often unable to attend to current circumstances, a problem that leads to exacerbation of symptoms. While there are promising preliminary data suggesting that tai chi leads to improvements in self-reported symptoms of PTSD, there are no data regarding the effects of tai chi on objective endocrine, physiological, and behavioral measures of PTSD.
The investigators hypothesize that the use of the mind-body practice of tai chi will lead to reductions in subjective self-report measures of PTSD as well a normalization of objective physiological correlates of PTSD. In particular, it is hypothesized that the efficacy of tai chi in the treatment of PTSD is hypothesized to be achieved by facilitating fear extinction and augmenting stress resilience through improved integration of mindfulness practices with daily physical activities. To test this hypothesis, the investigators propose the following specific aims:
• Specific Aim 1: To determine the self-reported symptom changes, behavioral changes, and physiological effects that take place during an 8-week intervention of simplified Tai Chi Moving Mindfulness Meditation and Resilience Training (TCMMMRT) in a population of police officers with and without self-reported PTSD. Results from these two groups will also be compared to a control group engaging in aerobic exercise.
- Self-reported outcome measures: Brief Pain Inventory (BPI) short form, Beck Depression Inventory (BDI), Pittsburgh Sleep Quality Index (PSQI), PTSD Checklist for Diagnostic and Statistical Manual of Mental Disorders (DSM-V) (PCL-5), and Canadian Occupational Performance Measure (COPM).
- Physiological outcome measures: Mobile Acoustic startle Reflex-monitoring System (MARS) measures, heart rate variability (HRV), cortisol measurements, and actigraphy to monitor sleep patterns and activity levels.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Maryland
-
Baltimore, Maryland, United States, 21224
- Johns Hopkins Bayview Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
For inclusion as a healthy control or a participant with PTSD:
- working in law enforcement
- between the ages of 18 and 65
- Both men and women
For inclusion as a participant with PTSD:
- previously diagnosed with PTSD by a medical professional (For inclusion in the PTSD group)
- Must meet criteria for PTSD as determined by the PCL-5 instrument on the day of initial assessment.
Exclusion criteria:
- taking sedative or stimulant drugs daily
- physical illness, injury, or disability preventing safe execution of low impact aerobic exercise
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: TCMMMRT First
Participants will perform an instructor-led mind-body exercise regimen 1 day per week during this arm of the study for a total of 8 weeks.
Home practice will be logged.
At the completion of the TCMMMRT Condition, participants will perform an instructor-led low impact aerobic exercise regimen 1 day per week for a total of 8 weeks.
Home exercise will be logged.
|
Low-impact mind-body exercise adapted from traditional tai chi.
Low-impact aerobic exercise, led by instructor
|
|
Active Comparator: Aerobic Exercise First
Participants will perform an instructor-led low impact aerobic exercise regimen 1 day per week during this arm of the study for a total of 8 weeks.
Home exercise will be logged.
At the completion of the aerobic exercise condition, participants will perform an instructor-led mind-body exercise regimen 1 day per week for a total of 8 weeks.
Home practice will be logged.
|
Low-impact mind-body exercise adapted from traditional tai chi.
Low-impact aerobic exercise, led by instructor
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in PCL-5 Score
Time Frame: Assessed on Day 1, Day 56, Day 112, and Day 168
|
Score on the PTSD Symptom Checklist for DSM-5.
The PTSD Checklist for DSM-5 (PCL-5) is a 20-item self-report measure that assesses the presence and severity of PTSD symptoms.
Items on the PCL-5 correspond with DSM-5 criteria for PTSD.
The PCL-5 can be used to quantify and monitor symptoms over time, to screen individuals for PTSD, and to assist in making a provisional or temporary diagnosis of PTSD.
|
Assessed on Day 1, Day 56, Day 112, and Day 168
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in BPI score
Time Frame: Assessed on Day 1, Day 56, Day 112, and Day 168
|
Brief Pain Inventory - a 9 item self-administered questionnaire used to assess pain severity and the affect of pain on daily functioning.
Contains four measures of pain severity on a 0-10 scale and pain interference with 7 life activities on a 0-10 scale.
It also includes items to specify pain location and treatments attempted.
Across all numbered scales, higher numbers indicate more pain.
|
Assessed on Day 1, Day 56, Day 112, and Day 168
|
|
Change in BDI score
Time Frame: Assessed on Day 1, Day 56, Day 112, and Day 168
|
Beck Depression Inventory - a 21 item assessment of depressive symptoms.
Raw score of 0-13 indicates minimal depression, 14 to 19 indicates mild depression, 20-28 indicates moderate depression, 29-63 indicates severe depression.
|
Assessed on Day 1, Day 56, Day 112, and Day 168
|
|
Change in PSQI score
Time Frame: Assessed on Day 1, Day 56, Day 112, and Day 168
|
Pittsburgh Sleep Quality Index - a 19 item assessment of different aspects of sleep that yields seven component scores and one component score.
The composite scores range from 0 to 21, where lower scores denote a healthier sleep quality.
Components are subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction.
|
Assessed on Day 1, Day 56, Day 112, and Day 168
|
|
Change in COPM score
Time Frame: Assessed on Day 1, Day 56, Day 112, and Day 168
|
Canadian Occupational Performance Measure - a semi-structured interview that enables assessment of occupational performance problems.
It results in two scores of participant-perceived levels of occupational performance.
It results in two main scores, performance and satisfaction, each out of 10, with higher numbers reflecting greater performance and satisfaction.
|
Assessed on Day 1, Day 56, Day 112, and Day 168
|
|
Change in Salivary Cortisol
Time Frame: Assessed on Day 1, Day 56, Day 112, and Day 168
|
Cortisol level in mcg/dL obtained from saliva sample.
|
Assessed on Day 1, Day 56, Day 112, and Day 168
|
|
Change in Heart Rate Variability
Time Frame: Assessed on Days 1, 7, 14, 21, 28, 35, 42, 49, 56, 63, 70, 77, 84, 91, 98, 105, 112, and Day 168
|
Heart Rate Variability collected using non-invasive Actigraph.
Beat to beat intervals will be recorded by the device and output as the standard deviation of nearest neighbor (SDNN) and the square root of the means of the squares of the successive differences between adjacent nearest neighbors (RMSSD).
|
Assessed on Days 1, 7, 14, 21, 28, 35, 42, 49, 56, 63, 70, 77, 84, 91, 98, 105, 112, and Day 168
|
|
Change in Acoustic Blink Response
Time Frame: Assessed on Days 1, 7, 14, 21, 28, 35, 42, 49, 56, 63, 70, 77, 84, 91, 98, 105, 112, and Day 168
|
Response to an acoustic tone (milliseconds from tone to eye blink) collected using the Mobile Acoustic startle Reflex-monitoring System (MARS) device
|
Assessed on Days 1, 7, 14, 21, 28, 35, 42, 49, 56, 63, 70, 77, 84, 91, 98, 105, 112, and Day 168
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Una McCann, Johns Hopkins University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB00226155
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Post Traumatic Stress Disorder
-
Acacia ClinicsElectroCore INC; Vagus Nerve SocietyRecruitingPTSD | Post Traumatic Stress Disorder | Post Traumatic Stress Disorders | Post-traumatic Stress Disorder (PTSD) | Post Traumatic Stress Disorder PTSD | PTSD - Post Traumatic Stress Disorder | Post-Traumatic Stress Disorder, PTSDUnited States
-
University of LuxembourgQuresta, Inc.; National Psychological Association of Ukraine; Veteran Mental...RecruitingPost Traumatic Stress Disorder | Post Traumatic Stress Disorder PTSD | Post-Traumatic Stress Disorder, PTSDUkraine
-
Istanbul UniversityRecruitingComplex Post-Traumatic Stress Disorder (CPTSD) | Post-traumatic Stress Disorder (PTSD)Turkey
-
Istanbul UniversityRecruitingComplex Post-Traumatic Stress Disorder (CPTSD) | Post-traumatic Stress Disorder (PTSD)Turkey
-
University of California, Los AngelesDefense Advanced Research Projects Agency; Defense Group, Inc.CompletedPost-traumatic Stress Disorder | Post-Traumatic Stress Disorder, ChronicUnited States
-
University of California, Los AngelesWithdrawnPost-traumatic Stress Disorder | Post-Traumatic Stress Disorder in ChildrenUnited States
-
IWK Health CentreRecruitingPost-Traumatic Stress Disorder in Adolescence | Post-Traumatic Stress Disorder, PTSD | Post-Traumatic Stress Disorder in YouthCanada
-
Weill Medical College of Cornell UniversityCompletedPost-traumatic Stress Disorder | Complex Post-Traumatic Stress DisorderUnited States
-
University of UtahEunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedPost-Traumatic Stress Disorder in Children | Post-Traumatic Stress Disorder in AdolescenceUnited States
-
University of ZurichCompletedPost Traumatic Stress Disorder (PTSD) | Complex Post-Traumatic Stress Disorder (CPTSD)Switzerland
Clinical Trials on Tai Chi Moving Mindfulness Meditation and Resilience Training
-
National Institute of Nursing Research (NINR)TerminatedHealthy | Obesity | AdultUnited States
-
Touro University NevadaActive, not recruitingWeight Loss | MetabolismUnited States
-
University of BernSwiss Federal Institute of TechnologyCompletedStress | Primary Prevention | Adult | Tai jiSwitzerland
-
Stanford UniversityWithdrawnCystitis, InterstitialUnited States
-
University of Texas Southwestern Medical CenterNational Institute on Aging (NIA)CompletedVentricular FunctionUnited States
-
Massachusetts General HospitalNational Center for Complementary and Integrative Health (NCCIH)Not yet recruitingStress Management and Meditative Movements for Asian Americans With Depression and Physical SymptomsMental Health (Depression) | Depression / Major Depressive Disorder
-
West Virginia UniversityCompletedStress | Burnout | Compassion Fatigue | MindfulnessUnited States
-
The Hong Kong Polytechnic UniversityCompletedMigraine DisorderHong Kong
-
Pacific UniversityNational Institutes of Health (NIH); National Center for Complementary and...RecruitingAggression | Stress, Psychological | Problem DrinkingUnited States
-
University of California, Los AngelesNational Institutes of Health (NIH); National Center for Complementary and...Completed