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Exercise training in PoTS – 20 years after our randomised trial
In 2005 we showed that three months of endurance training improves orthostatic intolerance. What two decades of research have added – and why the answer is no longer simply “train more”.
Prim. Priv.-Doz. Dr. Robert Winker, first author of the 2005 trial · October 2026
2005: a randomised trial in young soldiers
At the Medical University of Vienna we screened 2,768 military recruits for orthostatic intolerance with a questionnaire and tilt-table testing and found 36 cases. Thirty-one of them entered a randomised controlled trial: three months of jogging versus no training. At the end, only 6 of 16 trained participants still met the criteria for orthostatic intolerance, compared with 10 of 11 in the control group (p = 0.008), and their symptom score fell from 1.79 to 1.04 while the controls did not change. Our conclusion was that endurance training should be considered part of the treatment of orthostatic intolerance. Two honest caveats: the participants were young men, and “orthostatic intolerance” in 2005 was a broader label than PoTS by today’s criteria.
From our research · Hypertension 2005
After three months: who still had orthostatic intolerance?
Filled dot = criteria still met · grey = no longer met
Symptom score (lower = better): training 1.79 → 1.04 · control 2.09 → 2.14
2010–2016: the “small heart” and the Texas training programme
Benjamin Levine’s group in Dallas then explained why training works. Patients with PoTS had a smaller left ventricular mass (median 1.26 vs. 1.45 g/kg) and a lower blood volume (60 vs. 71 ml/kg) than healthy controls – a picture resembling deconditioning. In a head-to-head trial, three months of training improved symptoms, haemodynamics and quality of life, whereas the beta-blocker propranolol did not. Short-term training raised stroke volume and lowered the heart rate at any given workload. The key practical idea from these studies: start horizontally – rowing, swimming, recumbent cycling – so that patients can train without the upright posture that provokes their symptoms, and move to upright exercise only as fitness improves.
When the same programme was rolled out through an international registry in a community setting, 103 of 251 enrolled patients completed it – and 71 % of those who completed no longer met the PoTS criteria. The heart-rate rise on standing fell from 46 to 23 beats per minute, and in the 31 patients followed for 6–12 months the effect persisted. The drop-out rate is part of the result: more than half did not finish.
Guidelines and the state of the evidence
The 2015 Heart Rhythm Society consensus and the 2019 NIH expert meeting put exercise training, together with fluids, salt and compression, at the start of treatment, before any medication – and both noted that no drug is approved for PoTS and that the evidence for most drugs is thin. A 2018 meta-analysis in Mayo Clinic Proceedings found only three small randomised trials among 28 studies and rated each treatment class as “moderately effective” at best. A 2025 systematic review of randomised trials counted 21 trials with 750 patients in total over 23 years. The most recent review in JAMA (2026) still lists structured, supervised aerobic training as first-line therapy. In short: the direction of the evidence has not changed since 2005, but it is built on small studies, and the 2025 Frontiers review rightly points out that we know more about heart rates than about symptom burden and daily function.
What has changed: the dose is individual
The second decade of research is about how to train. A 2023 randomised trial compared a semi-supervised programme with personalised intensity and progression against standard advice: peak oxygen uptake rose by 3.4 ml/kg/min in the training group and did not change with standard care, exercise tolerance improved, and 80 % of trained patients had a delayed onset of symptoms during exercise. Remote and home-based programmes have been shown to be feasible and acceptable (the UK PULSE trial, 2025; a Swedish 200-patient trial is under way), and clinicians who treat severely affected, house- or bed-bound patients argue for individualised, remotely supervised programmes rather than fixed protocols. The message is not “exercise more” but “exercise at the right dose, with progression guided by symptoms”.
The big change since 2020: post-COVID PoTS and ME/CFS
COVID-19 has produced a large new group of PoTS patients. In a Swedish cohort of 467 highly symptomatic long-COVID patients, PoTS was common, affected mainly younger women, and came with lower physical activity and a shorter six-minute walking distance. Many of these patients also meet the criteria for myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS), and recent work shows that long COVID and ME/CFS share the same autonomic phenotype.
This matters for training. The hallmark of ME/CFS is post-exertional malaise (PEM): a marked worsening of symptoms 12 to 48 hours after physical or mental exertion that lasts days. Muscle studies suggest that impaired perfusion and sodium/calcium overload in skeletal muscle may underlie this intolerance. For these patients a graded exercise programme can cause harm, which is why the 2021 NICE guideline for ME/CFS advises against graded exercise therapy and recommends energy management – “pacing” – instead. The guideline is contested by some researchers, and the debate is genuinely open; but in practice the precautionary rule is clear: no fixed progression in a patient with PEM.
Does that mean no exercise at all? Not necessarily. A 2024 Swedish feasibility study offered 26 patients with post-COVID PoTS twelve weeks of individually dosed endurance and strength training with weekly physiotherapist support: 76 % adherence, 96 % completed, no safety problems, and symptoms and function improved. The difference to the 2005 protocol is the dose: symptom-contingent, heart-rate guided, often recumbent, and stopped or reduced at the first sign of PEM.
How I approach it today
- Confirm the diagnosis and exclude mimics – active stand or tilt test, ECG, blood tests, echocardiogram where indicated; thyroid, adrenal, anaemia, medication effects.
- Screen for PEM before any exercise advice. Two questions and, if in doubt, a symptom diary over two weeks decide which path we take.
- PoTS without PEM: fluids and salt, compression, then a stepwise programme starting horizontally (recumbent bike, rowing, swimming) three to five times a week, progressing to upright exercise over months; strength training for the legs; heart-rate guided intensity; medication (e.g. beta-blocker, ivabradine, midodrine) only where symptoms demand it.
- PoTS with PEM / ME/CFS: pacing first – staying below the individual exertion threshold, planned rest, heart-rate monitoring; gentle recumbent activity only as tolerated and with supervision; never “push through”.
- Review: standing test, symptom score and activity level after 8–12 weeks; adjust the dose, not the goal.
Unsure which group you belong to?
Take the self-check · How do I recognise PoTS? · Online consultation for international patients
Sources (PubMed)
Winker R, Barth A, Bidmon D, et al. Endurance exercise training in orthostatic intolerance: a randomized, controlled trial. Hypertension 2005;45:391–8. DOI
Fu Q, VanGundy TB, Galbreath MM, et al. Cardiac origins of the postural orthostatic tachycardia syndrome. J Am Coll Cardiol 2010. DOI
Fu Q, VanGundy TB, Shibata S, et al. Exercise training versus propranolol in the treatment of the postural orthostatic tachycardia syndrome. Hypertension 2011. DOI
Shibata S, Fu Q, Bivens TB, et al. Short-term exercise training improves the cardiovascular response to exercise in the postural orthostatic tachycardia syndrome. J Physiol 2012. DOI
Sheldon RS, Grubb BP, Olshansky B, et al. 2015 Heart Rhythm Society expert consensus statement on the diagnosis and treatment of postural tachycardia syndrome, inappropriate sinus tachycardia, and vasovagal syncope. Heart Rhythm 2015. DOI
George SA, Bivens TB, Howden EJ, et al. The international POTS registry: Evaluating the efficacy of an exercise training intervention in a community setting. Heart Rhythm 2016. DOI
Wells R, Spurrier AJ, Linz D, et al. Efficacy of therapies for postural tachycardia syndrome: a systematic review and meta-analysis. Mayo Clin Proc 2018. DOI
Fu Q, Levine BD. Exercise and non-pharmacological treatment of POTS. Auton Neurosci 2018. DOI
Vernino S, Bourne KM, Stiles LE, et al. POTS: State of the science and clinical care from a 2019 NIH Expert Consensus Meeting – Part 1. Auton Neurosci 2021. DOI
Raj SR, Arnold AC, Barboi A, et al. Long-COVID postural tachycardia syndrome: an American Autonomic Society statement. Clin Auton Res 2021. DOI
Wheatley-Guy CM, Shea MG, Parks JK, et al. Semi-supervised exercise training program more effective for individuals with postural orthostatic tachycardia syndrome in randomized controlled trial. Clin Auton Res 2023. DOI
Trimble KZ, Switzer JN, Blitshteyn S. Exercise in postural orthostatic tachycardia syndrome: focus on individualized exercise approach. J Clin Med 2024. DOI
Svensson A, Svensson-Raskh A, Holmström L, et al. Individually tailored exercise in patients with postural orthostatic tachycardia syndrome related to post-COVID-19 condition – a feasibility study. Sci Rep 2024. DOI
McGregor G, Sandhu H, Bruce J, et al. Exercise rehabilitation for people with postural tachycardia syndrome at two secondary care centres in the UK: the PULSE feasibility randomised controlled trial. BMJ Open 2025. DOI
Cortez MM, Nagi Reddy SK, Goodman B, et al. Impact of exercise to treat postural orthostatic tachycardia syndrome: a systematic review. Front Neurol 2025. DOI
Kwok CS, et al. The evidence for treatments for postural orthostatic tachycardia syndrome: a systematic review of randomized trials. Trends Cardiovasc Med 2025. DOI
Björnson M, et al. Prevalence and clinical impact of postural orthostatic tachycardia syndrome in highly symptomatic long COVID. Circ Arrhythm Electrophysiol 2025. DOI
Novak P, et al. Shared autonomic phenotype of long COVID and myalgic encephalomyelitis/chronic fatigue syndrome. PLoS One 2026. DOI
Scheibenbogen C, Wirth KJ. Key pathophysiological role of skeletal muscle disturbance in post COVID and myalgic encephalomyelitis/chronic fatigue syndrome. J Cachexia Sarcopenia Muscle 2025. DOI
Vink M, Vink-Niese A. The draft updated NICE guidance for ME/CFS highlights the unreliability of subjective outcome measures in non-blinded trials. J Health Psychol 2021. DOI
White P, et al. Anomalies in the review process and interpretation of the evidence in the NICE guideline for chronic fatigue syndrome and myalgic encephalomyelitis. J Neurol Neurosurg Psychiatry 2023. DOI
Chung TH, et al. Postural Orthostatic Tachycardia Syndrome (POTS): A Review. JAMA 2026. DOI
This article reflects the author’s reading of the literature as of October 2026 and is general medical information; it does not replace an individual consultation.