The Effect of ACT and Float REST on Burnout Syndrome.
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03535493 |
|
Recruitment Status :
Terminated
(Ethics Committee concerns.)
First Posted : May 24, 2018
Last Update Posted : August 29, 2018
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Burnout Syndrome | Behavioral: Acceptance and Commitment Therapy (ACT) Behavioral: Float REST Behavioral: ACT + Float REST | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 45 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Other |
| Official Title: | The Effect of Acceptance and Commitment Therapy (ACT) and Float REST (Restricted Environmental Stimulation Therapy) on Burnout Syndrome. |
| Actual Study Start Date : | June 1, 2018 |
| Actual Primary Completion Date : | August 27, 2018 |
| Actual Study Completion Date : | August 27, 2018 |
| Arm | Intervention/treatment |
|---|---|
| Active Comparator: Acceptance and Commitment Therapy (ACT) |
Behavioral: Acceptance and Commitment Therapy (ACT)
An ACT session entails a mindfulness-based training to foster and nurture effective behavioral and emotional responding to distress. |
| Active Comparator: Float REST |
Behavioral: Float REST
A float session entails laying supine in a light-proof, sound-proof tank consisting of a shallow pool of water (approximately 10 inches set to approximately 94.5 degrees to match skin temperature) with a high concentration of Epsom salt (approximately 1200 pounds) for 60 minutes.
Other Name: Float Therapy, Isolation Tank, Sensory Deprivation Tank |
| Experimental: ACT + Float REST |
Behavioral: ACT + Float REST
The combined intervention will combine ACT and Float REST. An ACT session entails a mindfulness-based training to foster and nurture effective behavioral and emotional responding to distress. A float session entails laying supine in a light-proof, sound-proof tank consisting of a shallow pool of water (approximately 10 inches set to approximately 94.5 degrees to match skin temperature) with a high concentration of Epsom salt (approximately 1200 pounds) for 60 minutes. |
- Assessing Change in Maslach Burnout Inventory - Human Services Survey (MBI-HSS) [ Time Frame: Metric will be used as screening prior to study intervention; continuous measurement at week 2, week 4, week 6, week 8 and at one month follow-up. ]A 22 item scale that measures depersonalization, emotional exhaustion, and personal accomplishment. It is designed for professionals in human services in an array of occupations including nurses, physicians, health aides, social workers, health counselors, therapists, police, correctional officers, clergy, and other fields focused on helping people live better lives by offering guidance, preventing harm, and ameliorating cognitive, emotional, or physical problems.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | Child, Adult, Older Adult |
| Accepts Healthy Volunteers: | Yes |
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03535493
| United States, Illinois | |
| International Behavioral Research Institute | |
| Saint Charles, Illinois, United States, 60174 | |
| Responsible Party: | Amrinder Babbra, Principal Investigator, International Behavioral Research Institute |
| ClinicalTrials.gov Identifier: | NCT03535493 |
| Other Study ID Numbers: |
IBRI |
| First Posted: | May 24, 2018 Key Record Dates |
| Last Update Posted: | August 29, 2018 |
| Last Verified: | August 2018 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
|
Syndrome Burnout, Psychological Disease |
Pathologic Processes Stress, Psychological Behavioral Symptoms |

