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The Effects of Passive Heat Therapy in Patients With Chronic Kidney Disease

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Completed

Conditions

Renal Insufficiency, Chronic

Treatments

Procedure: Thermoneutral Control (CON)
Procedure: Whole-body Passive Heat Therapy (HT)

Study type

Interventional

Funder types

Other

Identifiers

NCT05924919
22-01741 (Other Grant/Funding Number)
HM20024906

Details and patient eligibility

About

The objective of this proposal is to investigate the acute effects of whole-body passive heat therapy using far-infrared technology on vascular function, exercise capacity, and renal function in CKD patients. The central hypothesis is that an acute bout of whole-body passive heat therapy will be well-tolerated and lead to acute improvements in large blood vessel (macrovascular) function, small blood vessel (microvascular) function, and exercise capacity without significantly altering markers of acute kidney injury.

Enrollment

10 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for participants with CKD:

  • Age > 18 years old
  • Stage 2-4 CKD

Exclusion Criteria for participants with CKD:

  • Unstable medical conditions characterized by frequent or unpredictable biological, chemical, or psychological changes
  • Uncontrolled hypertension
  • Current fluid restrictions
  • End stage kidney disease or currently on dialysis treatment
  • Body weight < 40kg
  • Exhibits any contraindications to exercise as per ACSM guidelines
  • Regular tobacco and/or nicotine use
  • History of heat-related illness
  • Participates in regular exercise and/or sauna use
  • Current hormone replacement therapy
  • Pacemaker or electro-medical implant
  • Persons with or at risk of intestinal disorders including gastroporesis
  • History of diverticula
  • Persons who have undergone surgical procedures in the GI tract
  • Swallowing disorders
  • Chron's disease
  • Current pregnancy
  • Inability to provide informed consent

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Experimental Arm: Whole-body Passive Heat Therapy (HT)
Experimental group
Description:
Heat therapy will be administered using an infrared sauna. The intervention duration will last 25 minutes at a temperature of 60°C.
Treatment:
Procedure: Whole-body Passive Heat Therapy (HT)
Procedure: Thermoneutral Control (CON)

Trial contacts and locations

1

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Central trial contact

Danielle Kirkman, PhD; Domenico Chavez, MS

Data sourced from clinicaltrials.gov

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