Whole-body Hyperthermia for Depression

Not Applicable

Recruiting

• Conditions: Major Depressive Disorder
• Interventions: Device: Sham whole-body hyperthermia; Device: Active whole-body hyperthermia

• Registration Number: NCT06323785
• Lead Sponsor: University of Zurich

Brief Summary

The goal of this clinical trial is to test the efficacy of whole-body hyperthermia in major depression. The main question it aims to answer is:

• Does whole-body hyperthermia alleviate symptoms of depression?

Participants will be randomised to sham or active whole-body hyperthermia. The study will last 6 weeks during which five visits will take place. Depression will be measured repeatedly and biological mechanisms will be investigated.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2024-02-28
• Study First Submitted QC: 2024-03-14
• Study First Posted: 2024-03-21
• Status Verified: 2024-06
• Last Update Submitted: 2024-06-10
• Last Update Posted: 2024-06-11
• Study Start: 2024-06-15
• Primary Completion: 2026-03-01
• Study Completion: 2026-03-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

• mental capacity to make decisions
• informed consent signed by the subject
• fluent in the German language
• 18-65 years of age
• pre-menopausal women: willing to use birth control or not to engage in sexual intercourse for the duration of the study (the latter only in the case that this corresponds to the habitual lifestyle of this person)
• fulfil DSM-5 criteria for a major depressive episode
• score ≥ 14 on the Hamilton Rating Scale for Depression (HAMD-17; minimum: 0, maximum: 68, higher scores indicate higher depression)
• the major depression is the primary mental disorder

Exclusion Criteria

• vulnerable subjects
• known or suspected non-compliance, drug or alcohol abuse within the past 2 years
• inability to follow the procedures of the investigation, e.g. due to language problems, psychological disorders, dementia, etc. of the subject
• participation in another investigation with an investigational drug or another MD within the 30 days preceding and during the present investigation
• previous enrolment into the current investigation
• enrolment of the Sponsor-Investigator, her family members, employees and other dependent persons
• contraindications and limitations of the MD as described in the instructions for use
• BMI > 30
• lifetime schizophrenia, lifetime bipolar disorder, current catatonic or psychotic symptoms, current suicidal ideation, current severe claustrophobia, anorexia or bulimia nervosa within the past 5 years
• metallic, silicone, or saline implants
• cardiovascular conditions or problems, including uncontrolled hypertension, congestive heart failure, or documented evidence of coronary artery disease
• chronic conditions/diseases associated with a reduced ability to initiate thermoregulatory cooling, including Parkinson's, multiple sclerosis, central nervous system tumors, and diabetes with neuropathy
• history of peripheral circulatory disease, including peripheral vascular disease and deep vein thrombosis
• history of a cerebral vascular accident
• history of epilepsy or cerebral aneurisms
• cancer in the last five years, except for resected non-melanoma skin cancer
• any clinically significant autoimmune disease
• hemophilia or proneness to bleeding
• fever the day of study intervention
• hypersensitivity to heat
• recent acute joint injury
• enclosed infections, be they dental, in joints, or in any other tissues
• any other medical condition or disorder that is unstable and clinically significant, or that could interfere with the accurate assessment of safety or efficacy of treatment
• intake of medication interfering with thermoregulatory cooling, including barbiturates, diuretics, beta-blockers, and anti-histamines
• intake of psychotropic medication within 2 weeks (8 weeks for fluoxetine)
• need for psychotropic medication during the study period
• current psychotherapy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Sham whole-body hyperthermia	Sham whole-body hyperthermia	-
Active whole-body hyperthermia	Active whole-body hyperthermia	-

Primary Outcome Measures

Name	Time	Method
Hamilton Rating Scale for Depression (HAMD-17; minimum: 0, maximum: 68, higher scores indicate higher depression)	1 week	Depressive symptoms (observer-rated)

Secondary Outcome Measures

Name	Time	Method
Hamilton Rating Scale for Depression (HAMD-17; minimum: 0, maximum: 68, higher scores indicate higher depression)	6 weeks	Depressive symptoms (observer-rated)
Medical Outcomes Study 36-item short-form health survey (MOS-SF; minimum: 0, maximum: 100, higher scores indicate better health status)	1 week and 6 weeks	Quality of life
Beck Depression Inventory (BDI; minimum: 0, maximum: 63; higher scores indicate higher depression)	1 week and 6 weeks	Depressive symptoms (self-reported)

Trial Locations

Locations (1)

University of Zurich, Institute of Psychology; 🇨🇭 Zurich, Switzerland