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Hemodynamic-guided nonpharmacologic management of orthostatic hypotension

Nonpharmacologic management of orthostatic hypotension based on hemodynamic profiles - Nonpharmacologic management of orthostatic hypotension based on hemodynamic profiles

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059401
Enrollment
75
Registered
2025-10-15
Start date
2025-11-17
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

High-risk conditions for orthostatic hypotension: neurological disorders, cardiovascular diseases, kidney failure, COPD, hypertension, diabetes mellitus, fragility fractures, and deconditioning.

Interventions

Sponsors

Shinshu University
Lead Sponsor
Tokyo Bay Rehabilitation Hospital Fujita Health University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age between 65 and 90 years 2. Having one or more of the following diseases as a primary diagnosis or comorbidity: Neurological disorders (stroke, spinal cord injury, head trauma, brain/spinal cord tumor, neurodegenerative diseases, demyelinating diseases, peripheral autonomic neuropathy, etc.) Cardiovascular diseases (heart failure, atrial fibrillation, myocardial infarction, etc.) Kidney failure COPD Hypertension Diabetes mellitus Fragility fractures Deconditioning 3. At least one week has elapsed since hospital admission 4. Expected hospital stay of at least four weeks 5. Sufficient cognitive and language function to understand instructions for the experimental procedures 6. Able to provide written informed consent from the participant or a legally authorized representative for participation in this study

Exclusion criteria

Exclusion criteria: 1. Unable to perform a head-up tilt test due to joint contractures, pain, or other physical limitations 2. Currently undergoing or scheduled to begin treatment for osteoporosis 3. Presence of abdominal aortic aneurysm detected on abdominal screening at admission, history of thoracoabdominal surgery within the past 2 months, tube feeding, or gastrostomy 4. Presence of cardiac pacemaker, prosthetic joint, or other metallic implants 5. Unable to maintain standing position for at least 3 minutes even with a tilt table due to severe dizziness or syncope 6. Unable to measure blood pressure on the upper arm due to humeral fracture, post-mastectomy status, or other reasons 7. Unable to undergo abdominal compression due to skin injury, itching, or discomfort around the pelvic area 8. Restricted from mobilization or exercise per attending physician's order 9. Any other condition deemed inappropriate for study participation by the attending physician or principal investigator

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure

Secondary

MeasureTime frame
Diastolic blood pressure Mean arterial pressure Heart rate Stroke volume index Cardiac index Total peripheral resistance index Visual analogue scale score

Countries

Japan

Contacts

Public ContactKazuaki Oyake

Shinshu University Department of Physical Therapy

k_oyake@shinshu-u.ac.jp0263372413

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026