A Randomised Controlled Trial Of Day Hospital And Day Centre Rehabilitation
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Original research Functional electrical stimulation assisted
Apr 29, 2021 unit (ICU) stay into an assessor-blinded single centre randomised controlled trial to receive either FESCE-based protocolised or standard rehabilitation that continued up to day 28 or ICU discharge. Results We randomised in 1:1 ratio 150 patients (age 61±15 years, Acute Physiology and Chronic Health
Patient self-management in primary care patients with mild
Trial registration: Current controlled trials ISRCTN06710391. Keywords: COPD, Self-management, Physical activity, Randomised controlled trial * Correspondence: [email protected] 3Department of Public Health, Epidemiology and Biostatistics, University of Birmingham, Birmingham, UK Full list of author information is available at the end of the
Multifactorial intervention for hip and pelvic fracture
Methods/design: This dual-centre, randomised controlled trial compares a multifactorial intervention with usual care as control condition. Two hundred and forty community-dwellers (≥ 65years) with a hip or pelvic fracture and mild to moderate cognitive impairment (MMSE 17 26) are recruited at the end of inpatient rehabilitation.
Effect of early supervised progressive resistance training
A single-blinded randomised controlled trial encouraged to take active part in the treatment and rehabilitation. On surgery day patients were admitted to hospital
Central Adaptation of Pain Perception in Response to
controlled trial found no change in PPT of the ref-erence site, the sternum bone (11), a small-scale study with weaker methods observed increased PPT of a non-trained reference muscle (22). Thus, the influence of central adaptations of pain perception in response to rehabilitation of musculoskeletal pain remains unclear.
Comparison of a structured home-based rehabilitation
Mar 07, 2016 We conducted an assessor-blinded, non-inferiority, randomised controlled trial comparing centre-based PR with a home-based programme supported with the SPACE for COPD manual with the primary endpoint at 7 weeks, and follow-up at 6 months. The study took place between November 2007 and July 2012. All
Effectiveness of rehabilitation intervention in persons with
Objective: A stratified, randomised, waitlist controlled study over 12 months assessed the effectiveness of rehabilitation in persons with multiple sclerosis (MS) in an Australian community cohort. Methods: Patients with definite MS (n=101) recruited from a tertiary hospital database, randomised to a
Physical Fitness Training in Patients with Subacute Stroke
Multicentre, randomised controlled, endpoint blinded trial. SETTING Seven inpatient rehabilitation sites in Germany (2013-17). PARTICIPANTS 200 adults with subacute stroke (days 5-45 after stroke) with a median National Institutes of Health stroke scale (NIHSS, range 0-42 points, higher values indicating more severe strokes) score of 8
Effects and costs of real-time cardiac telerehabilitation
costs. Therefore, a two-arm parallel randomised controlled non-inferiority experimental design was chosen. The trial protocol was submitted for registration before enrolling participants (www. anzctr.org.au, ACTRN12614000843651) and has been published7; no changes were made during the trial. All participants provided written consent.
Day clinic vs. hospital care of pneumonia and severe
Day clinic vs. hospital care of pneumonia and severe malnutrition in children under ﬁve: a randomised trial Hasan Ashraf 1,† , Nur H. Alam 1 , Marufa Sultana 1 , Selina A. Jahan 1 , Nurshad Begum 1 , Sharmin Farzana 1 ,
Safety and efficacy of co-careldopa as an add-on therapy to
and physical therapy during early rehabilitation after stroke. Methods This double-blind, multicentre, randomised controlled trial of co-careldopa versus placebo in addition to routine NHS occupational and physical therapy was done at 51 UK NHS acute inpatient stroke rehabilitation services.
Evaluation of a smartwatch-based intervention providing
Phase 2: Pilot randomised controlled trial phase Phase two was a single-blind, pilot randomised con-trolled trial; with the research assessor blinded to the group allocation (it was not possible to blind the ward staff and patients). Group allocation was performed by an independent researcher using a 1:1 allocation ratio. A
Effects of inspiratory muscle training on dyspnoea in severe
pulmonary rehabilitation: controlled randomised trial Marc Beaumont1, Philippe Mialon2, Catherine Le Ber1, Patricia Le Mevel1, Loïc Péran1, Olivier Meurisse1, Capucine Morelot-Panzini3, Angelina Dion4 and Francis Couturaud5 Affiliations: 1Pulmonary Rehabilitation Unit, Morlaix Hospital Centre, EA3878, European University of
Does feedback on daily activity level from a Smart watch
during inpatient stroke rehabilitation and the short-term effects on simple functional activities, primarily mobility. Methods/design: A randomized controlled trial will be undertaken within the stroke rehabilitation wards of the Second Affiliated hospital of Anhui University of Traditional Chinese Medicine, Hefei, China. The study participants
The Birmingham rehabilitation uptake maximisation study (BRUM
Jan 29, 2008 hospital services and drug use for secondary prevention and employment status. Travel costs and time were based on distances from patients addresses to the relevant centre. Hospital records were used to check the number of attendances at the hospital rehabilitation programmes of trial participants and self reported hospital admission data.
Rationale and design of a randomised clinical trial for an
Methods: In this single centre randomised controlled trial 120 patients with an absolute indication for cardiac rehabilitation will be randomised in a 1:1 ratio to an intervention group with 6 months of heart rate based telemonitoring guidance or a control group with traditional follow-up after cardiac rehabilitation. The primary endpoint will
Early home-supported discharge for patients with stroke in
Stroke, early home-supported discharge, randomised controlled trial, Functional Independence Measure, clinical effectiveness, home rehabilitation, Portugal, care continuity Received: 20 May 2015; accepted: 19 December 2015
Open Access Protocol Early initiation of post-sternotomy
randomised controlled trial and economic evaluation. BMJ Open 2018;8:e019748. doi:10.1136/ bmjopen-2017-019748 Received 22 September 2017 Revised 13 February 2018 Accepted 23 February 2018 1Department of Cardiac Rehabilitation, Centre for Exercise and Health, University Hospital, Coventry, UK 2Cardiff Centre for Exercise and Health, Cardiff
Statistical Analysis Plan for a multi-centre randomised
Statistical Analysis Plan for a multi-centre randomised controlled trial: Management of Refeeding Syndrome in Critical Illness Gordon S. Doig,1 Fiona Simpson,2 and Philippa T. Heighes3. on behalf of the Refeeding Syndrome Trial Management Committee. The Refeeding Syndrome Trial
Early, goal-directed mobilisation in the surgical intensive
hospital and ICU days, fewer days to ﬁ rst day out of bed, and better functional mobility at hospital discharge. On our last search, using the same criteria, we found two randomised controlled studies, both published since 2015, on early mobilisation in patients in the ICU, in two diﬀ erent cohorts (patients with ARDS and those with stroke).
A self-management programme for COPD: a randomised controlled
This was a single-centre, investigator-blinded, randomised controlled trial conducted with 6 months follow-up, which took place from December 2009 to April 2012. Participants were randomised to SPACE FOR COPD or usual care. All participants gave written informed consent and ethical approval for the study was granted by
A randomised controlled trial of expressive arts-based
A randomised controlled trial of expressive arts-based intervention for young stroke survivors Caitlin Kar Pui Chan1, Temmy Lee Ting Lo2, Adrian Ho Yin Wan1, Pamela Pui Yu Leung3, Marco Yiu Chung Pang4 and Rainbow Tin Hung Ho1,2* Abstract Background: Stroke causes lasting brain damage that has numerous impacts on the survivor s physical
Day Hospital Rehabilitation: Effectiveness And Cost In The
The effectiveness and cost of day hospital care in rehabilitation were studied in a randomised controlled trial in 120 elderly patients who were assessed at referral and six weeks and five months later in activities of daily living skills and mood. Day hospital patients were compared with a control group, who were
Reablement in community-dwelling older adults: a randomised
Trial registration: The trial was registered in ClinicalTrials.gov November 20, 2012, identifier NCT02043262. Keywords: Rehabilitation, Activities of daily living, Older adults, COPM, Randomised controlled trial Background The growth in the ageing population, in combination with an expected shortage of health-care personnel in
Rehabilitation of older patients: day hospital compared with
A randomised controlled trial. Trusts that were found to provide both home-based and day hospital rehabilitation were contacted to ascertain interest in participating in the trial. A total of 19 sites expressed initial interest and eventually four sites were recruited to carry out a pragmatic RCT in which patients were
Activities and participation of children and adolescents
randomised controlled trial design [42 45]. The Brains Ahead! Study, using a randomised controlled trial and a large multicentre prospective cohort, is, to the authors knowledge, the first to examine the effect of a psychoe-ducational intervention on long-term activity and par-ticipation outcomes in children and adolescents who
Long-term integrated telerehabilitation of COPD Patients: a
An international multicentre randomised controlled trial (RCT) conducted across sites in three countries (Norway, Australia, and Denmark), where 120 patients with COPD are randomly assigned to three arms (tele-rehabilitation, treadmill, control) in a 1:1:1 ratio and followed up for 2 years. The trial is restricted to pa-
Rehabilitation of older patients: day hospital compared with
Rehabilitation of older patients: day hospital compared with rehabilitation at home. A randomised controlled trial SG Parker,1,2* P Oliver,3 M Pennington,4 J Bond,4 C Jagger,5 PM Enderby,3 R Curless,6 T Chater,3 A Vanoli,4,7 K Fryer,1 C Cooper,3 S Julious,3 C Donaldson,4 C Dyer,8 T Wynn,9 A John1 and D Ross1
A feasibility study of a randomised controlled trial to
Trial feasibility was defined as the successful recruitment and retention of trial participants, adherence to the intervention, identification of barriers to the intervention, and the rigorous collection of outcome data. Methods: A prospective, single-centre, randomised controlled feasibility study was conducted. Thirty adult
RESEARCH ARTICLE Open Access Early supported discharge after
in order to compare the rehabilitation results after ESD to rehabilitation as usual and to investigate the effect of community treatment given in two different settings; either in a day unit (ESD 1) or in the patients homes (ESD 2). We therefore designed a randomised controlled trial with two different ESD arms and one control arm,
Statistical Analysis Plan for a multi-centre randomised
Guided by the findings 1of a cluster randomised controlled trial, we initiated and conducted a multi-centre, Phase II, randomised controlled trial (RCT) to determine if the provision of a continuous supplementary infusion of a standard mixture of L -amino acids protects the kidney from acute injury during critical illness.
PAPER Multidisciplinary rehabilitation for people with
May 29, 2002 Methods: The study was a randomised controlled crossover trial comparing patients and carers who had received rehabilitation four months before assessment with those who had not. Patients were recruited from a neurology clinic, attended a day hospital from home weekly for six weeks using pri-
An evaluation of the effectiveness and cost effectiveness of
Method A pragmatic randomised controlled trial with nested economic evaluation of 2160 inactive participants with coronary heart disease risk (CHD, 1559, 72%), mild to moderate depression, anxiety or stress (79, 4%) or both (522, 24%) randomised to receive (1) NERS or (2) normal care and brief written information.
Open Access Research Femoral Nerve Block Intervention in Neck
This was a pragmatic, two-arm randomised controlled trial in a single centre. The study was registered with EudraCt (ref: 2010-023871-25 (17/02/2011)) and ISRCTN: ISRCTN92946117. There was a delay in trial registration due to administration oversight, but no changes in the protocol were made between first patient recruitment and trial registration.
A randomised controlled trial to investigate the use of high
A randomised controlled trial to investigate the use of high-frequency airway oscillations as training to improve dyspnoea in COPD Enya Daynes 1,2,3, Neil Greening1,2,3, Salman Siddiqui2,3 and Sally Singh1,2,3 Affiliations: 1Centre of Exercise and Rehabilitation Sciences, Glenfield Hospital, Leicester, UK. 2NIHR
Randomised, clinically controlled trial of intensive
Central Hospital is the only place for referral for specialist care in the region. In this randomised, clinically controlled trial, community dwelling patients with acute hip fractures aged 65 years or older were randomly assigned to two rehabilitation groups after surgery at the hospital. All patients were living independently and had
Reducing utilisation of hospital services by case management
Hospital, 8 Haven of Hope Road, Tseung Kwan O, Kowloon, Hong Kong, China. [email protected] Reducing utilisation of hospital services by case management: a randomised controlled trial Antony CT Leung, Daniel CN Yau, Chi-pun Liu, Chak-sum Yeoh, Tak-yi Chui, Iris Chi and Nelson WS Chow What is known about the topic?
Evaluating rehabilitation following lumbar fusion surgery
Design of trial Rehabilitation following fusion surgery (REFS) is a ran-domised, controlled, multi-method, single-centre, feasi-bility trial. Participants (inclusion and exclusion criteria) A convenience sample of subjects (n = 50) will be re-cruited from the Neurosurgical Department of the Na-tional Hospital for Neurology and Neurosurgery, (NHNN,
Vojta therapy improves postural control in very early stroke
An overview of the trial schedule (interventions and visits) is provided in Table 1. The Trunk Control Test (TCT) [23 27] the measurement of the primary end-point - was assessed at day 2 after admission to the hospital before the first treatment (baseline), at day 5 and day 9 after treatment. The TCT is a validated test to
Cervicovestibular rehabilitation in sport-related concussion
rehabilitation and cervical spine physiotherapy decreased the time until medical clearance in individuals with prolonged postconcussion symptoms. Methods This study was a randomised controlled trial. Consecutive patients with persistent symptoms of dizziness, neck pain and/or headaches following a sport-related concussion (12 30 years, 18