None listed
Conditions
Brief summary
This study aims to assess the benefit of accessing 16 weeks of IT in addition to standard care for people with traumatic neurological spinal, brain or proximal limb injury when transitioning from being an inpatient to outpatient. We propose that people will experience improved management of their mental health and wellbeing, pain, physical function, and socialisation than those who do not undertake IT.
Interventions
The study proposes to use a mixed model design including a randomised controlled trial (RCT) design for both quantitative and qualitative (self-report) outcomes and then to conduct qualitative semi-structured interviews with a representative sub-group of participants. The RCT will use a wait-list control whereby participants are randomised to receive 16 weeks of IT immediately upon enrolment or after a 16 week wait. Outcome measures will be assessed at weeks 0, 16 and 32 allowing the RCT comparison as well as a non-randomised crossover analysis (in wait-listed participants) and a single group prospective 16 week follow up (in intervention group). The intervention will be the standard Immersion Therapy (IT) service model delivered by accredited IT Specialists (who are also Accredited Exercise Physiologists). IT is an underwater experience for people living with injury, chronic illness and/or disability, TBI, SCI, as well as chronic pain, mental illness, and developmental and degenerative disorders. Using scuba equipment (a buoyancy control device and regulator or full-face mask) in a two-to-five-metre deep pool environment, clients can swim, walk, play or relax, completely immersed. IT does not aim to teach clients to dive recreationally but utilizes scuba as a form of ‘therapy’, aiming to exert its effects, either through physical movement underwater and/or the psychosocial experience. Participants will be introduced to the service at their own pace in accordance with existing protocols and given complete independence in designing their service in collaboration with their clinician. The treating clinicians will liaise with other service providers as appropriate to ensure the service can complement the person’s rehabilitation goals. Participants will be asked to attend at least 1 and up to 2 session per week for 16 weeks with each session lasting up to 45 minutes. Sessions will be conducted in a one-on-one format, with participant attendance recorded through the service provider’s (Determined2) existing booking system. Attendance will be monitored weekly by the service provider’s Operations Manager to ensure adherence. The IT will take place at The Parks Recreation & Sports Centre, 46 Cowan Street, Angle Park, SA. Semi-structured, one-on-one interviews will be conducted by a member of research team either face-to-face or via video conferencing and at take 45 to 60 minutes. All participants that have completed the IT program will be invited to participate in the interviews until the sample size is sufficient that novel data become so infrequent that further interviews are unlikely to meaningfully alter the results. Interviews will be audio recorded with participant consent and transcribed using a professional transcription service.
Sponsors
Study design
Eligibility
Inclusion criteria
Are between 18 and 65 years old. Have experienced a traumatic injury resulting in permanent impairment to neurological function (brain, spinal cord or upper/lower limb). Are within 12 months of discharge from inpatient rehabilitation. Understand spoken and written English.
Exclusion criteria
Do not pass the IT Medical Exam. Not able to attend one session of IT each week for 16 weeks Are participating in non-standard (as determined by research team senior clinicians) treatment or activities that significantly overlap with IT (ie significant additional physical activity/exercise or water-based treatment).