Chronic Pain Skills Study - Vanderbilt University Medical Center
Status: | Recruiting |
---|---|
Conditions: | Chronic Pain, Chronic Pain |
Therapuetic Areas: | Musculoskeletal |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/24/2019 |
Start Date: | June 22, 2017 |
End Date: | October 22, 2019 |
Contact: | Lindsey C McKernan, Ph.D. |
Email: | research.ocim@vanderbilt.edu |
Phone: | (615) 875-9990 |
The Osher Center for Integrative Medicine (OCIM) at Vanderbilt is a multidisciplinary
outpatient clinic treating patients with chronic pain and complex health issues via
integrative services, with goals of improving overall health and wellbeing of those served.
At OCIM, clinical hypnosis has been historically provided on an individual basis by the
investigator. Due to its impact and increased patient demand for this service, the
investigator will be conducting group hypnosis services in addition to individual services
order to expand the reach of this program to participants. As such, the investigators see
this as a tremendous opportunity to contribute to clinical research to contribute to the
evidence based for this form of service by examining participant-reported outcomes associated
with completing the treatment. For this project, the investigators seek to assess the impact
of a manualized group treatment protocol utilizing clinical hypnosis as a treatment for
chronic pain. The investigators will be evaluating participant-reported outcomes to assess
the 1) feasibility of conducting hypnosis in this setting 2) impact of group hypnosis on pain
and 3) how participants' responsiveness to hypnosis impacts treatment outcome.
outpatient clinic treating patients with chronic pain and complex health issues via
integrative services, with goals of improving overall health and wellbeing of those served.
At OCIM, clinical hypnosis has been historically provided on an individual basis by the
investigator. Due to its impact and increased patient demand for this service, the
investigator will be conducting group hypnosis services in addition to individual services
order to expand the reach of this program to participants. As such, the investigators see
this as a tremendous opportunity to contribute to clinical research to contribute to the
evidence based for this form of service by examining participant-reported outcomes associated
with completing the treatment. For this project, the investigators seek to assess the impact
of a manualized group treatment protocol utilizing clinical hypnosis as a treatment for
chronic pain. The investigators will be evaluating participant-reported outcomes to assess
the 1) feasibility of conducting hypnosis in this setting 2) impact of group hypnosis on pain
and 3) how participants' responsiveness to hypnosis impacts treatment outcome.
Inclusion Criteria:
1. 18 years of age or older; *
2. Self-reported presence of chronic pain;**
3. Average pain intensity rating of ≥ 3 on a 0-10 Numerical Rating Scale (NRS) of pain
intensity in the last week; **
4. Worst pain intensity rating of ≥ 5 on a 0-10 Numerical Rating Scale (NRS) of pain
intensity in the last week;**
5. Duration of chronic pain 3 months or more; **
6. Experiences pain at least 75% of the time in the past 3 months; Those who have a hard
time answering this question will be asked the following question: "Which statement
best describes your pain?"
1. Pain all the time, but the pain intensity varies;
2. Pain most of the time with only occasional periods of being pain-free;
3. Pain that comes and goes;
4. Occasional pain; Participants must report experiencing pain that matches one of
the first two options;**
7. Able to read, speak, and understand English.**
Exclusion Criteria:
1. Cognitive impairment or limitations (i.e. history of moderate to severe Traumatic
Brain Injury (TBI), unresolved TBI, or other medical condition) that would interfere
with a patient's ability to participate in a group involving focused attention*.
2. Current or history of diagnosis of primary psychotic or major thought disorder as
listed in participant's medical record or self-reported within the past five years;*
3. Hospitalization for psychiatric reasons other than suicidal ideation, homicidal
ideation, and/or PTSD self-reported or noted in chart (within the past 5 years);*
4. Psychiatric or behavioral conditions in which symptoms are unstable or severe (e.g.
current delirium, mania, psychosis, suicidal ideation, homicidal ideation, substance
abuse dependency) as listed in participant's medical record or self-reported within
the past six months;*
5. Any behavioral issues as noted in the medical record or by a provider that would
indicate the participant may be inappropriate in a group setting;***
6. Presenting symptoms at time of screening that would interfere with participation,
specifically active suicidal ideation with intent to harm oneself or active delusional
or psychotic thinking;**
7. Difficulties or limitations communicating over the telephone;**
8. Any planned life events that would interfere with participating in the key elements of
the study.**
9. Reported average daily use of >120mg morphine equivalent dose (MED). **
- also verified via medical record review, as described below. **verified solely
via self-report, as described below; there is no medical record
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