Engaging Veterans Seeking Service-Connection Payments in Pain Treatment

让寻求服务连接付款的退伍军人参与疼痛治疗

• 批准号: 10013125
• 负责人: Marc I Rosen
• 金额: $ 130.24万
• 依托单位: YALE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-09-20 至 2024-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10013125
• 关键词: Age; Alcohol or Other Drugs use; Algorithms; Award; Back; Behavior; Brief Pain Inventory; Caring; Chronic; Clinical; Clinical Trials; Communication; Conduct Clinical Trials; Cost Analysis; Counseling; Distress; Early Intervention; Electronic Health Record; Evaluation; Financial compensation; Health Promotion; Healthcare Systems; Human Resources; Individual; Injury compensation; Institutional Review Boards; Intervention; Interview; Joints; Measures; Mediating; Mediator of activation protein; Medical Records; Medical center; Military Personnel; Multi-Institutional Clinical Trial; Musculoskeletal; Musculoskeletal Diseases; Nail plate; Natural Language Processing; Neck; New England; Opioid; Outcome; Outcome Assessment; Outcome Measure; Pain; Pain interference; Pain management; Patient Self-Report; Phase; Populations at Risk; Preparation; Procedures; Professional counselor; Protocols documentation; Quality of life; Randomized; Records; Risk; Secure; Services; Severities; Site; Site Visit; Source; Telephone; Testing; Text; Toxicology; Veterans; base; chronic pain; cost effective; cost effectiveness; cost estimate; design; early phase clinical trial; effectiveness testing; experience; functional improvement; high risk; implementation strategy; improved; informant; innovation; motivational enhancement therapy; multimodality; pain outcome; pain reduction; pain relief; pain symptom; payment; pragmatic trial; primary outcome; psychologic; recruit; screening; screening, brief intervention, referral, and treatment; secondary outcome; service utilization; structured data; substance abuse treatment; substance misuse; symptomatic improvement; treatment as usual; willingness to pay

Abstract In 2015 alone, 97,223 new Veterans under age 35 began receiving compensation for injuries related to their military service. In total, there are 559,999 post-9/11 Veterans being compensated for back or neck conditions, and a partially overlapping 596,250 for limitation of flexion in joints. Veterans seeking compensation for musculoskeletal conditions often develop chronic pain and are at high risk for substance misuse. Early intervention is needed to arrest worsening pain and risky substance use, particularly among post-9/11 Veterans for whom engagement in non-pharmacological pain treatment has the potential to improve their overall quality of life and spare them the complications of opioid treatments. The service-connection application is an ideal point-of-contact for initiating early intervention treatments for these at-risk Veterans. We propose to test the effectiveness and cost-effectiveness of Screening, Brief Intervention and Referral to Treatment for Pain Management (SBIRT-PM), designed to reduce pain and risky substance use. In brief, the counselor explains that treating both physical and psychological aspects of pain leads to the best outcomes, outlines what VA (and non-VA if preferred) services are available to Veterans, explains that substances are sometimes used for pain relief, and segues into traditional SBIRT. SBIRT-PM's efficacy is supported by a completed clinical trial of 101 Veterans applying for service-connection for MSD, and by studies showing the efficacy of SBIRT for people with risky substance use and of Motivational Interviewing for engagement in non-pharmacological pain care. The study will involve a two-year period to arrange for clinicians at a single “hub” site to counsel Veterans throughout New England by phone with SBIRT-PM, and a four-year period to conduct the clinical trial and disseminate its findings. During the two-years of preparation for the clinical trial, the team will prepare SBIRT-PM for implementation by establishing communication (Relational Coordination is the theoretical framework) between the “hub” where the SBIRT-PM clinician is sited and the “spoke” sites, establishing study- related procedures, and piloting the intervention at each of the eight VA medical centers in New England. For the full clinical trial, we will randomize 1200 Veterans applying for compensation related to MSD to either SBIRT-PM or Usual Care (UC) across eight VA medical centers in New England. Outcome assessment by phone will occur at 12 and 36-week follow-ups, and will be corroborated with other sources of information ---the electronic health record and toxicology testing of nail clippings. We hypothesize that, compared to Usual Care, SBIRT-PM will be more effective and cost-effective in improving Veterans' pain and substance use. We further hypothesize that a mediator of these improvements will be use of non-pharmacological services, as extracted from VA records from structured data fields and from narrative text in the medical record using an innovative natural language processing algorithm. Screening and referral to treatment at service-connection examinations can transform a widely-used point of entry to VA into a health-promoting encounter.

摘要