Skip to content

Home Orthostatic Training in Chronic Fatigue Syndrome

Home Orthostatic Training in Chronic Fatigue Syndrome: a randomised controlled feasibility study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN89726128
Enrollment
50
Registered
2009-06-22
Start date
2008-01-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic fatigue syndrome Nervous System Diseases Encephalitis, myelitis and encephalomyelitis

Interventions

Patients will receive routine clinical care including withdrawal of potential culprit medications, and conservative and abortive advice as is our usual practice. Following full written consent they wi

Sponsors

Newcastle upon Tyne Hospitals NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Chronic fatigue syndrome (CFS)/myalgic encephalomyelitis (ME) patients 2. Both males and females, aged 18 years and over 3. Patients who fulfil the Fukuda diagnostic criteria 4. Patients with an autonomic phenotype, i.e., have a composite autonomic symptom scale of greater than 32.5

Exclusion criteria

Exclusion criteria: 1. Inability to give informed consent 2. Patients on drugs which can affect the autonomic nervous system which cannot be discontinued safely 3. Inability to stand for up to 40 minutes due to muscular or neurological disorders, cardiac transplantation, or pregnancy

Design outcomes

Primary

MeasureTime frame
1. Study compliance. Timepoints: 1 week, 4 weeks, 6 months. 2. Autonomic function. Timepoints: baseline, 1 week, 4 weeks, 6 months.

Secondary

MeasureTime frame
Fatigue. Timepoints: baseline, 1 week, 4 weeks, 6 months.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026