None listed
Conditions
Brief summary
The study aims to explore the feasibility and acceptability of a new outpatient Transitional Pain Management Clinic at St Vincent's Hospital for participants with risk factors for ongoing pain and opioid use after surgery or injury. The intervention will include three sessions with a pain medicine physician and three sessions with a pain physiotherapist over a three month period post-discharge from hospital. The study will also evaluate the relationship between completion of the intervention at the Transitional Pain Management Clinic key outcomes including pain-associated disability, opioid use, and healthcare utilisation. It is anticipated that this clinic will be feasible to implement and acceptable to patients. Given that this clinic is aimed at prevention and early-intervention before the development of persistent postsurgical and posttraumatic pain, significant changes in key pain-associated outcomes are not necessarily anticipated.
Interventions
This is a longitudinal pilot study aiming to assess the feasibility of a multidisciplinary Transitional Pain Management Service for participants discharged from St Vincent's Hospital Sydney following surgery or traumatic injury. Participants with risk factors for persistent post-surgical or post-traumatic injury pain will be recruited from the Acute Pain Service as inpatients. They will then attend the outpatient St Vincent's Hospital Transitional Pain Management Service face-to-face or via Telehealth, attending three sessions each with a specialist pain medicine physician and a pain physiotherapist (at 1 month, 2 months and 3 months post discharge). Specialist pain medicine physician consultations will be 30 minutes duration and include: Assessment of biomedical recovery following surgery or injury: - Full history and physical examination of relevant systems - Detailed pain history including trajectory of acute pain, plus other chronic pain problems, including numerical rating scale reports of worst, average and best pain Assessment of biomedical complications: - e.g Evidence of wound infection, thromboembolism, other post surgical complications Assessment of medication use (including opioid medications): - Both pre and post surgery/injury Assessment of functional recovery in personal, employment, social domains: - e.g. Assessment of personal and domestic activities of daily living, return to work, leisure activities Assessment of mental health and substance use: - e.g. Assessment of mood, anxiety, other mental health problems - e.g. Assessment of interpersonal relationships - e.g. Assessment of substance use including alcohol and tobacco Referral to other health services if appropriate: - e.g. To surgical teams if surgical complications, to mental health services if significant mood issues. All sessions will be recorded by contemporaneous notes in the participant's medical file, and a letter outlining each consultation will be sent to their nominated primary care physician. Physiotherapy sessions will 1 hour for the initial consultation and 30mins for subsequent consultations, and will be delivered by a specialized pain physiotherapist. Sessions will include: Assessment and identification of risks or barriers that may hinder a return to presurgery/preinjury level of functioning, e.g: - Fear avoidant behaviours - Unhelpful motor patterns - Anxiety with movement - Unhelpful thinking patterns - Sleep disturbance - Lack of support from family and/or friends - Home environment barriers e.g. no appropriate modifications or aids Functional outcome measures as appropriate for each participant e.g: - Timed up and go test (TUG) - 6 minute walk test (6MWT) - 30 second chair stand test (30 CST) - Near tandem stance test - Wall push ups in 1 min Depending on individual participant context, other physiotherapy may include but is not limited to: Pain education e.g: - What to expect as recovery progresses, expectation setting regarding pain especially with movement, non-pharmacological techniques to manage pain including pacing education, modification of movement/use of aids and up-titration of activity as healing progresses Exercise therapy: - Exercise therapy will be trialed during the consultation and a smart watch will be worn by the patient to ensure exercise intensity is under 70% of maximum heart rate Balance training Goal setting - As per NSW Agency for Clinical Innovation SMART guidelines for goal setting - https://aci.health.nsw.gov.au/chronic-pain/brain-injury/understanding-pain/goal-setting- and-maintaining-the-changes Relaxation therapy Correcting unhelpful motor patterns Addressing fear avoidant behaviours Education on pacing Education on scheduling daily activities appropriate to stage of recovery Providing online/print resources Sleep hygiene General dietary advice Referrals to other health professionals / services e.g: - When a patient presents with any condition that is outside the scope of physiotherapy practice such as undiagnosed fractures, tendon / ligament rupture, mental illness eg depression. To monitor adherence to the intervention, patients will complete an exercise recording sheet/ diary which will be assessed in subsequent sessions for issues/progress. All physiotherapy sessions will be recorded by contemporaneous note taking in the patient's medical file. Participants will be asked to complete online self-report questionnaires at baseline and 3-month, 6-month, and 12-month follow ups, which will include: Demographic data Medical history Healthcare utilization Medication use Brief Pain Inventory (BPI) Depression Anxiety Stress Scales (DASS21) Pain Self-Efficacy Questionnaire Pain Catastrophising Scale (PCS) Tampa Scale of Kinesiophobia (TSK) The questionnaires will take approximately 15-30 minutes to complete.
Sponsors
Study design
Eligibility
Inclusion criteria
Participants will include those who are 18 years and over, are patients of the St Vincent’s Hospital Acute Pain Service (APS), and meet the one or more of the following eligibility criteria: Patients with a history of preadmission chronic pain conditions Patients with a history of pre-admission opioid use <60mg oral morphine equivalents (OMEDD) as calculated by the ANZCA Faculty of Pain Medicine Opioid Calculator Severe pain during hospital admission as assessed by the APS High opioid consumption on discharge, >90mg OMEDD Patients discharged with a prescription for long-acting opioid preparations Psychological risk factors including depression, anxiety, pain catastrophizing, and kinesiophobia.
Exclusion criteria
Participants currently receiving opioid maintenance therapy (e.g. buprenorphine or methadone) Patients with active substance use disorder or dependence Pre-admission opioid use >60mg OMEDD Participants with psychotic mental health disorders, or extremely severe depression