E-health Resilience Program For Chronic Spine Pain
Status: | Recruiting |
---|---|
Conditions: | Back Pain, Orthopedic, Pain |
Therapuetic Areas: | Musculoskeletal, Orthopedics / Podiatry |
Healthy: | No |
Age Range: | 18 - 70 |
Updated: | 10/17/2018 |
Start Date: | August 9, 2018 |
End Date: | August 30, 2019 |
Contact: | Sana Shaikh, MD |
Email: | skazi@med.umich.edu |
Phone: | 734-763-5526 |
A Randomized Controlled Trial of an E-health Resilience Program For Chronic Spine Pain
This study will examine a e-health resilience based program, JOOL, for chronic spine pain
patients through the following aims:
Aim 1: To test the effectiveness of a resilience based program known as JOOL Aim 2: To
evaluate the characteristics of the participants most likely to benefit from this treatment
patients through the following aims:
Aim 1: To test the effectiveness of a resilience based program known as JOOL Aim 2: To
evaluate the characteristics of the participants most likely to benefit from this treatment
This is a pilot RCT in which 150 patients with chronic spine pain will be randomized to one
of two arms: (1) a group that downloads the JOOL mobile application resilience program; and
(2) a control group.The primary outcome will be a change in physical function.
of two arms: (1) a group that downloads the JOOL mobile application resilience program; and
(2) a control group.The primary outcome will be a change in physical function.
Inclusion Criteria:
- Patient of the UM Back & Pain Center
- Primary diagnosis of neck or back pain (spine pain)
- Age 18-70
- English speaking
- Able to provide consent
- Willing to download the mobile application and comply with study procedures
- Antidepressant medications stable for ≥ 4 weeks
- No plan to initiate a new non-pharmacological pain intervention during the 30-day
study period (e.g. back surgery, physical therapy, behavioral therapy
Exclusion Criteria
- Having known psychotic disorder or the presence of another psychiatric condition (e.g.
severe depression [HADS scores ≥ 15], suicidal ideation) or cognitive impairment (e.g.
severe dyslexia, TBI) limiting ability to give consent and/or participate fully in the
study
- Currently undergoing psychotherapeutic care at the Back & Pain Center because many of
the concepts that are the focus of this study are already employed in that treatment
- Other factors that at the discretion of the investigators would adversely affect study
participation.
We found this trial at
1
site
Ann Arbor, Michigan 48106
Principal Investigator: Afton Hassett, PsyD
Phone: 734-763-5226
Click here to add this to my saved trials