Multiple Sclerosis-Collaborative Approach to Rehabilitation Effectiveness Study (MS-CARE)
Multiple Sclerosis, Pain, Depression
About this trial
This is an interventional treatment trial for Multiple Sclerosis focused on measuring multiple sclerosis, pain, depression
Eligibility Criteria
Inclusion Criteria:
- Patient has a definitive diagnosis of MS confirmed by subjects' MS physician in the University of Washington (UW) MS Center;
- Patient has received care and plans to continue to receive care at the UW MS Center during enrollment period;
- Patient has access to and is able to communicate over the telephone (we will provide phone headsets if needed) to allow participation in the telehealth components of the study;
- Patient can read, speak and understand English;
- Patient is at least 18 years of age.
- Patient reports a clinically significant problem with pain and/or depression.
Exclusion Criteria:
- Patient represents a high suicide risk;
- Patient reports symptoms of a current psychotic disorder or diagnosis of bipolar disorder with current psychotic features at time of screening;
- Subject attends appointments more than once per month with a psychiatrist for treatment of depression;
- Patient reports planning major surgery in the next ten months;
- Patient reports alcohol or psycho-active substance dependence within past month;
- Patient has moderate to severe cognitive impairment.
Sites / Locations
- University of Washington- Harborview Medical Center
- University of Washington Medicine MS Center
- University of Washington-Health Sciences Building
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Collaborative Care (CC)
Usual Care
Collaborative care (CC) is a systematic and integrated approach to improving the delivery and utilization of effective treatments for chronic pain and depression. The care was delivered through an interdisciplinary team, organized around a CC manager (CCM) who guided the patient through various aspects of care during the 16-week treatment phase. The team also included the patient's MS physician and the CC Supervisors, a group of clinicians who were experts of the study domain . The CCM offered all subjects care management, collaborative medical management, and psychosocial treatment appropriate to their problem area (i.e., pain, depression, or both) described below. If the patient had both pain and depression, he or she received care management and collaborative medical management for both.
Subjects assigned to usual care were informed by the CCM of their depressive and pain symptoms and that they should consult with their MS or primary care provider about possible care for these conditions. Study personnel did not make any further attempts to influence usual care participants' depression or pain management unless a psychiatric emergency arose (e.g., suicidal ideation was detected at baseline or any of the outcome assessments).