Passive standing as an adjunct rehabilitation intervention after stroke: a randomized controlled trial
© Ferrarello et al. 2015
Received: 31 January 2015
Accepted: 9 April 2015
Published: 8 July 2015
Early physical rehabilitation enhances functional recovery in stroke survivors. Supported standing is a common adjunctive therapeutic practice in subjects with several central nervous diseases who are unable to stand actively. Data on the effect of supported positioning on standing frames in individuals with recent stroke are scarce and contradictory.
To verify if the addition of supported standing practice (SSP), delivered by means of a standing frame in two durations, to conventional physical therapy (CPT), may improve motor function, autonomy, and mobility in individuals with disability due to recent stroke.
After baseline assessment, 75 participants with severe disability due to stroke, all receiving CPT, were randomly assigned to adjunctive 20 or 40 min of SSP, or CPT only (control). Motor function, autonomy, and mobility were assessed before and after training, and three months later.
All participants assessed received the planned dose of intervention. No adverse events of SSP were detected. Most outcome measures improved from baseline through the end of treatment and in the follow-up in all groups; the extent of change was comparable across the three randomization groups.
In this randomized trial, SSP was unable to provide any sizeable adjunctive benefit, above and beyond CPT, in subjects with recent stroke.
KeywordsStroke Supported standing Randomized controlled trial
Stroke is a major cause of disability and death worldwide , with only a small proportion of survivors achieving full functional recovery after acute event. Indeed, at 40 % of survivors have difficulties in performing basic self-care tasks after 6 months , and more than 30 % report participation restrictions as long as 4 years after stroke . Systematic reviews show that organized multidisciplinary care and rehabilitation are effective in the early phase of a stroke, improving survival and independence, and reducing length of hospital stay and need for institutionalization .
Physical rehabilitation enhances substantially the functional recovery in stroke survivors, and improvements are greater with earlier beginning and higher intensity of rehabilitation . Early mobilization lessens the likelihood of acute phase complications (e.g., pneumonia, pressure sores, deep vein thrombosis) and usually begins when clinical conditions are stable . Beyond sitting, the standing position brings additional benefits such as prevention of hip and knee flexors contractures, circulatory training, autonomic nervous system stimulation, and sensory activation . Moreover, recovery of the ability to stand up and sustain load on the affected limb is crucial to gait training and recovery of upper limb functionality [8, 9]. Supported standing on tilt table or standing frame is an adjunctive therapeutic practice commonly adopted in subjects with several central nervous diseases who are unable to stand actively. Its aim is to improve antigravity muscles strength and head and trunk postural control, maintain standing ability, and prepare for gait training .
Data on the effect of supported positioning on standing frames in patients with recent stroke are scarce and contradictory. In a randomized controlled trial (RCT), 14 sessions of supported standing, added with flexible duration and schedules to conventional rehabilitation within nine weeks after stroke onset, did not significantly improve functional status . However, potential weaknesses should be recognized in this study: the intervention was administered late in the course of the disease, its intensity was low, its duration was left to the therapists’ discretion , and the first post-treatment assessment often did not coincide with the end of the intervention . In another pilot RCT, an intervention combining passive standing on a variety of stabilizers and task training, achieved some improvement in balance . Thus, we deemed as necessary a study conducted with more stringent selection criteria and a rigorously controlled intensity of the intervention, in order to ascertain the merit of passive standing in post-stroke rehabilitation.
We conducted the present RCT to verify whether the addition to early conventional physical therapy (CPT) of supported standing practice (SSP) delivered by means of a standing frame in two durations, improves motor function, autonomy, and mobility in individuals with disability due to recent stroke.
The reporting of this study conforms to the CONSORT (Consolidated Standards of Reporting Trials) Statement for non-pharmacologic trials . The study was approved by the IRCCS Fondazione Don Gnocchi ethics committee.
Persons with recent stroke, admitted for early rehabilitation to the inpatient Neurology Unit of the IRCCS Fondazione Don Gnocchi in Florence, Italy, from April 2011 to February 2012, were screened for enrollment. Inclusion criteria were: (1) first ever ischemic or hemorrhagic stroke, (2) age ≥18 years, (3) admission within 4 weeks from stroke onset, (4) severe functional limitation in walking (score 0 or 1 in the Functional Ambulation Classification, FAC) , (5) tolerance to the standing frame of at least 10 min (assessed two days after admission), (6) stable clinical conditions, (7) adequate participation and cognitive capacity, and (8) ability to provide informed consent.
Exclusion criteria were: (1) clinical contraindications to prolonged upright position (e.g. postural hypotension), (2) previous stroke, (3) severe limitations of the range of motion, particularly the lack of hip and knee extension, and ankle dorsiflexion, (4) the presence of recent fractures of the pelvis or lower limb (if full weight- bearing was not allowed) and (5) any other co-morbidity or disability that would preclude participation in the training program. Eligible subjects signed an informed consent conforming to the Helsinki Declaration, which contained detailed information on study design and data management.
Study design and procedures
After inclusion and baseline assessment, participants were stratified according to the FAC score (0 and 1). They were then randomly assigned to either adjunctive 20 or 40 min of SSP (experimental interventions), or standard (see below) CPT only (control). The random sequence was generated by an investigator not involved in participants’ assessment (MDB) using a web-based application (http://www.randomizer.org). Allocation assignment was kept concealed using serially numbered, opaque, sealed envelopes.
Baseline and follow-up evaluations were performed by an independent physical therapist (GD), blinded to group allocation and otherwise uninvolved in the study. Treatments were administered by physical therapists five days a week for three weeks, in an inpatient setting. Assessments were done at enrollment (T0), at the end of the 3-week treatment (T1), and three months later (T2).
A formal sample size calculation was not performed because of lack of adequate preliminary data on the expected effect size. In particular, the present RCT differed from previous studies in the outcome measures chosen, in the overall duration of the treatment period and in the double dosing (20 and 40 min/day) of the intervention.
Participants randomized to the 40-min daily SSP treatment received 2 20-min sessions (morning and afternoon). The standing frame STANDY (Ormesa®, www.ormesa.com) was utilized for the experiment. Equipped with heel rests, knee pads and back rest (both adjustable in width, depth, and height) it allows a flexible and safe static regimen.
Patients’ positioning on the standing and monitoring were conducted by the treating physical therapists. Exercise duration was timed and inconveniences or discomforts were recorded. The standing session was not performed, or could be interrupted, if participants showed intolerance or hypotension.
Conventional physical therapy treatment
All participants underwent individual CPT sessions, which included 60 min of neuromuscular and musculoskeletal interventions, and practice of functional activities . Moreover, 20 min of passive cycling (upper- and/or lower- limbs), hydrokinetic and occupational therapy were administered, as well as cognitive and speech therapy when needed.
Demographic and main clinical characteristics (stroke type, days from event, and affected side) were recorded. Stroke severity was assessed with the National Institute of Health Stroke Scale (NIHSS). The clinical history of participants was investigated for any contraindications to upright position. Goniometric measurement of the range of movement of the lower limbs was performed to exclude limitations that might affect the ability to stand. Moreover, the ability to control the trunk in an upright position (sitting and standing) was recorded. Tolerance to the standing frame was assessed by measuring blood pressure, heart and respiratory rate first in the supine and seated positions, and then after 5 min of standing. Signs and symptoms of hypotension were monitored. As a safety measure, blood pressure and heart rate were recorded also during the interventions.
Primary outcome measures
The Fugl-Meyer Assessment of Motor Recovery after Stroke - motor domain (FM) scale, the Functional Independence Measure (FIM), and the FAC were chosen as primary outcome measures.
The FM, used in both clinical and research settings, is one of the most widely used quantitative measures of motor impairment, with excellent intra- and inter- rater reliability and construct validity, particularly of the motor domain, as shown by numerous studies . The motor domain includes items measuring movement, coordination, and reflex action about upper- and lower- limb; motor score ranges from 0 (hemiplegia) to 100 points (normal motor performance), divided into 66 points for the upper extremity and 34 points for the lower extremity. The FIM measures the level of disability and indicates how much assistance is required to perform activities of daily living . The FAC categorizes subjects according to basic motor skills necessary for functional ambulation .
Secondary outcome measures
The Modified Ashworth scale (MAS), the Timed-Up-and-Go test (TUG) at three months (T2), the drop in systolic blood pressure from supine to standing position, and the ability to control the trunk while sitting or standing were taken as secondary outcome measures.
The MAS  evaluates spasticity in patients with lesions of the central nervous system; knee flexors and extensors, ankle dorsal and plantar flexors, and hip adductors of the affected side were assessed. The TUG is a widely used mobility test, which requires that a person rises from a chair, walks three meters, turns around, walks back to the chair, and sits down again on the chair, while being timed .
Moreover, the Trunk Control Test (TCT) , which examines four simple aspects of trunk movement, was added to the protocol after the study began, and was therefore administered in a subsample.
Data were analyzed by an independent investigator, blind to group allocation. Sample characteristics were analyzed by descriptive statistics. Differences between groups in baseline demographic and pre-training characteristics were examined using one-way ANOVA for continuous and the chi-square test for ordinal and categorical variables respectively, taking into account trends as appropriate. To perform the between-group comparisons, a two-way ANOVA for repeated measures with group x time interaction was used. The Kruskal-Wallis test was utilized to highlight the between-group differences in the TUG test three months after the end of treatment.
Analyses were performed according to the intention- to- treat (ITT) and the per- protocol (PP) principles . For ITT analysis missing data were dealt with by using the last- observation- carried- forward method . The IBM SPSS Statistics for Windows, (version 20.0; IBM Corp, Armonk, NY) was utilized for calculations. The significance level was set at a p value of <0.05.
Characteristics of the sample
Baseline characteristics of the study groups
(n = 20)
(n = 24)
(n = 31)
Days from event
Type of stroke I/E
Lesion side DX/SX
Trunk control upright No/Yes
Effects of experimental and conventional interventions
20’ SSP Group
40’ SSP Group
62. 15 (±3.18)
-2. 43 (±1.03)
Supported standing programs are routinely used in many settings, different clinical conditions and age groups . Being passively supported in the upright position by adaptive equipment is a common intervention for individuals who have inadequate postural control or lower limb strength . The stroke rehabilitation community showed interest in the topic, in fact in a systematic review exploring the issue in adults with upper motor neuron injury, slightly more than half of the participants in the studies included had stroke . Evidence related to the effectiveness of SSP in neurorehabilitation is controversial and few firm conclusions can be drawn from systematic reviews, limited to some positive effects reported in the presence of stabilized symptoms [10, 22, 23].
This study shows that the addition of SSP for 20 or 40 min to CPT, administered in an early phase, does not improve motor function, autonomy, and mobility in individuals with disability due to a stroke. Although outcome measures improved significantly from baseline through the end of treatment and in the follow-up, the extent of change was unrelated to the assignment group. At the same time, the SSP had no adverse effects.
These findings are consistent with those of the largest previous study on this issue , which had been considered as inconclusive because of methodological limitations, such as late application and poor standardization of the intervention [10, 11].
In our study, we tried to overcome some of the weaknesses that limited previous experiments [10–12], by narrowing the time gap to enrollment, standardizing and increasing the dose administered, and conducting the first post-treatment assessment soon at the end of the intervention. We administered the adjunctive SSP within 22 days from event and with a precise delivered dose, which might reflect clinical practice for adopted session duration, frequency, and assistive device .
As the comparisons with other studies are difficult, because baseline participants’ disability level or type of treatment administered were not similar [12, 24, 25], it was not possible to estimate the sample size in our RCT and, therefore, it is possible that our study is under-powered. However, the absence of any trend towards improvement and of a dose-effect relationship (40 min vs. 20 min SSP) in any of our outcome measures discourages the design of further RCTs with larger sample size.
In conclusion, this RCT failed to show any functional benefit of SSP in the rehabilitation of recent stroke. Nevertheless , enough support exists for the use of a standing device as part of a comprehensive 24-h postural management and activity program for individuals chronically ill with severely limited mobility . We cannot exclude that, as shown in other neurological conditions such as multiple sclerosis  or cerebral palsy , SSP might provide some benefit in the stabilized phase of the disease, to limit the impact of long-term complications on overall well-being and quality of life [27, 28]. However, large, high quality studies are required to definitively verify these potential, late positive effects, which have so far limited support from scientific evidence.
- Sacco RL, Kasner SE, Broderick JP, et al. An updated definition of stroke for the 21st century: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2013;44:2064–89.PubMedView ArticleGoogle Scholar
- Mayo NE, Wood-Dauphinee S, Cote R, Durcan L, Carlton J. Activity, participation, and quality of life 6 months poststroke. Arch Phys Med Rehabil. 2002;83:1035–42.PubMedView ArticleGoogle Scholar
- Gadidi V, Katz-Leurer M, Carmeli E, Bornstein NM. Long-term outcome poststroke: predictors of activity limitation and participation restriction. Arch Phys Med Rehabil. 2011;92:1802–8.PubMedView ArticleGoogle Scholar
- Ferrarello F, Baccini M, Rinaldi LA, et al. Efficacy of physiotherapy interventions late after stroke: a meta-analysis. J Neurol Neurosurg Psychiatry. 2011;82:136–43.PubMedView ArticleGoogle Scholar
- Pollock A, Baer G, Campbell P, et al. Physical rehabilitation approaches for the recovery of function and mobility following stroke. Cochrane Database Syst Rev. 2014;4:CD001920.PubMedGoogle Scholar
- Jauch EC, Saver JL, Adams Jr HP, et al. Guidelines for the early management of patients with acute ischemic stroke: a guideline for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2013;44:870–947.PubMedView ArticleGoogle Scholar
- Knecht S, Hesse S, Oster P. Rehabilitation after stroke. Dtsch Arztebl Int. 2011;108:600–6.PubMed CentralPubMedGoogle Scholar
- Mercer VS, Freburger JK, Chang SH, Purser JL. Measurement of paretic-lower-extremity loading and weight transfer after stroke. Phys Ther. 2009;89:653–64.PubMed CentralPubMedView ArticleGoogle Scholar
- Higgins J, Mayo NE, Desrosiers J, Salbach NM, Ahmed S. Upper-limb function and recovery in the acute phase poststroke. J Rehabil Res Dev. 2005;42:65–76.PubMedView ArticleGoogle Scholar
- Newman M, Barker K. The effect of supported standing in adults with upper motor neurone disorders: a systematic review. Clin Rehabil. 2012;26:1059–77.PubMedView ArticleGoogle Scholar
- Bagley P, Hudson M, Forster A, Smith J, Young J. A randomized trial evaluation of the Oswestry Standing Frame for patients after stroke. Clin Rehabil. 2005;19:354–64.PubMedView ArticleGoogle Scholar
- Allison R, Dennett R. Pilot randomized controlled trial to assess the impact of additional supported standing practice on functional ability post stroke. Clin Rehabil. 2007;21:614–9.PubMedView ArticleGoogle Scholar
- Boutron I, Moher D, Altman DG, Schulz KF. Ravaud P; CONSORT Group. Methods and processes of the CONSORT Group: example of an extension for trials assessing nonpharmacologic treatments. Ann Intern Med. 2008;148:W60–6.PubMedGoogle Scholar
- Viosca E, Martínez JL, Almagro PL, Gracia A, González C. Proposal and validation of a new functional ambulation classification scale for clinical use. Arch Phys Med Rehabil. 2005;86:1234–8.PubMedView ArticleGoogle Scholar
- Dejong G, Horn SD, Gassaway JA, Slavin MD, Dijkers MP. Toward a taxonomy of rehabilitation interventions: Using an inductive approach to examine the “black box” of rehabilitation. Arch Phys Med Rehabil. 2004;85:678–86.PubMedView ArticleGoogle Scholar
- Gladstone DJ, Danells CJ, Black SE. The fugl-meyer assessment of motor recovery after stroke: a critical review of its measurement properties. Neurorehabil Neural Repair. 2002;16:232–40.PubMedView ArticleGoogle Scholar
- Hamilton BB, Laughlin JA, Fiedler RC, Granger CV. Interrater reliability of the 7-level functional independence measure (FIM). Scand J Rehabil Med. 1994;26:115–9.PubMedGoogle Scholar
- Bohannon RW, Smith MB. Interrater reliability of a modified Ashworth scale of muscle spasticity. Phys Ther. 1987;67:206–7.PubMedGoogle Scholar
- Hafsteinsdóttir TB, Rensink M, Schuurmans M. Clinimetric properties of the Timed Up and Go Test for patients with stroke: a systematic review. Top Stroke Rehabil. 2014;21:197–210.PubMedView ArticleGoogle Scholar
- Collin C, Wade D. Assessing motor impairment after stroke: a pilot reliability study. J Neurol Neurosurg Psychiatry. 1990;53:576–9.PubMed CentralPubMedView ArticleGoogle Scholar
- Gupta SK. Intention-to-treat concept: A review. Perspect Clin Res. 2011;2:109–12.PubMed CentralPubMedView ArticleGoogle Scholar
- Glickman LB, Geigle PR, Paleg GS. A systematic review of supported standing programs. J Pediatr Rehabil Med. 2010;3:197–213.PubMedGoogle Scholar
- Paleg GS, Smith BA, Glickman LB. Systematic review and evidence-based clinical recommendations for dosing of pediatric supported standing programs. Pediatr Phys Ther. 2013;25:232–47.PubMedView ArticleGoogle Scholar
- Lee MY, Wong MK, Tang FT. Clinical evaluation of a new biofeedback standing balance training device. J Med Eng Technol. 1996;20:60–6.PubMedView ArticleGoogle Scholar
- Wong AM, Lee MY, Kuo JK, Tang FT. The development and clinical evaluation of a standing biofeedback trainer. J Rehabil Res Dev. 1997;34:322–7.PubMedGoogle Scholar
- Baker K, Cassidy E, Rone-Adams S. Therapeutic standing for people with multiple sclerosis: efficacy and feasibility. Int J Ther Rehabil. 2007;14:104–9.View ArticleGoogle Scholar
- Nordström B, Näslund A, Eriksson M, Nyberg L, Ekenberg L. The impact of supported standing on well-being and quality of life. Physiother Can. 2013;65:344–52.PubMed CentralPubMedView ArticleGoogle Scholar
- Nordström B, Nyberg L, Ekenberg L, Näslund A. The psychosocial impact on standing devices. Disabil Rehabil Assist Technol. 2014;9:299–306.PubMed CentralPubMedView ArticleGoogle Scholar
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