NCT06323785RecruitingNot Applicable
Randomised Sham-controlled Trial of Whole-body Hyperthermia for Depression
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- University of Zurich
- Enrollment
- 30
- Locations
- 1
- Primary Endpoint
- Hamilton Rating Scale for Depression (HAMD-17; minimum: 0, maximum: 68, higher scores indicate higher depression)
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to 65 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Arms & Interventions
Active whole-body hyperthermia
Active Comparator
Intervention: Active whole-body hyperthermia (Device)
Sham whole-body hyperthermia
Sham Comparator
Intervention: Sham whole-body hyperthermia (Device)
Outcomes
Primary Outcomes
Hamilton Rating Scale for Depression (HAMD-17; minimum: 0, maximum: 68, higher scores indicate higher depression)
Time Frame: 1 week
Depressive symptoms (observer-rated)
Secondary Outcomes
- Hamilton Rating Scale for Depression (HAMD-17; minimum: 0, maximum: 68, higher scores indicate higher depression)(6 weeks)
- 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)
- Beck Depression Inventory (BDI; minimum: 0, maximum: 63; higher scores indicate higher depression)(1 week and 6 weeks)
Investigators
Study Sites (1)
Loading locations...
Similar Trials
Completed
Not Applicable
Whole-body Hyperthermia for Mild to Moderate Depressive DisorderDepression, UnipolarNCT03906175Universität Duisburg-Essen46
Not yet recruiting
Not Applicable
Whole-Body Hyperthermia for Mood and Anxiety DisordersPostpartum AnxietyAnxiety DisordersMood DisordersPostpartum DepressionNCT06144294Weill Medical College of Cornell University240
Completed
Phase 3
Study of a Repetitive Transcranial Magnetic Stimulation (rTMS) Device for the Treatment of Major Depressive DisorderMajor Depressive DisorderNCT00104611Neuronetics286
Unknown
Not Applicable
Theta-Burst Stimulation in Major Depressive Episodes With Mixed Characteristics.Depressive DisorderDepressive EpisodeBipolar DisorderNCT04123301University of Sao Paulo90
Completed
Phase 2
Dose-finding Study With Lu AA24530 in Major Depressive DisorderMajor Depressive DisorderNCT00599911H. Lundbeck A/S652