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NCT07664540Not yet recruiting

Fasting, Exercise, and Diet to Activate Autophagy in Depression

Targeting Autophagy in Depression: Fasting, Exercise, Diet

Source: ClinicalTrials.gov · Last updated 24 Jun 2026

Brief summary (registry, in English)

Depression is a common mental health condition that affects millions of people worldwide and is a leading cause of disability. Although current treatments can be effective, many patients do not fully recover or experience long-term improvement. This study aims to better understand how lifestyle factors such as physical activity and diet-related processes may influence biological mechanisms that could be linked to depression. The study focuses on a natural cellular process called autophagy, which helps cells remove damaged components and maintain healthy function. Autophagy is influenced by energy availability in the body and may be affected by behaviors such as physical exercise and caloric restriction. Early evidence suggests that changes in autophagy may also be linked to mood regulation and depression, but this relationship is not yet well understood in humans. In this exploratory study, we will investigate how physical activity influences autophagy and related metabolic and molecular processes in healthy adults. We will also examine whether these effects differ between individuals with different body weight and fitness levels, and between women and men. A total of approximately 120 healthy adults aged 18 to 40 years will participate. Participants will be divided into four groups based on sex and body weight (normal weight or overweight). Each participant will attend study visits at the University Hospital Zurich and perform a standardized cycling exercise test under medical supervision. During the exercise test, participants will perform a graded cycling protocol that gradually increases in intensity until exhaustion. We will collect small blood samples from a vein and from a fingertip at several time points before, during, and after exercise. Saliva samples will also be collected to measure stress-related hormones. Additional measurements include heart rate, breathing parameters, oxygen consumption, and physical performance. Blood and saliva samples will be analyzed using advanced laboratory techniques to study changes in metabolism, immune signaling, hormones, gene activity, and markers related to autophagy. These analyses will help identify biological pathways that are activated by exercise and may be relevant to brain health and depression. Participants will undergo medical screening before inclusion to ensure safety. Individuals with certain medical conditions or factors that could interfere with the study results will not be included. Participation is voluntary, and participants may withdraw at any time without consequences. The study involves minimal risks associated with blood sampling and intense physical exercise, which will be performed under close medical supervision. The expected benefit is improved scientific understanding of how lifestyle-related biological processes may be linked to mental health, which could support the development of new preventive or therapeutic strategies for depression in the future.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
17 Jun 2026
Start date
11 Sept 2026
Primary completion date
30 Sept 2029
Lead sponsor
University of Zurich
Diseases
Depression
NCT number
NCT07664540

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From 11 Sept 2026 to the primary completion date, 30 Sept 2029
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • No infectious illness for at least two weeks prior to the test
  • No vitamin supplementation during the week prior to the performance test
  • No use of hormonal contraceptives in the last 6 months before the onset of the study (SG1/3)
  • having given birth within the 12 months before inclusion in the study (SG1/3)
  • regular use of medication other than thyroxine
  • surgery less than 4-6 months ago

Other illness

  • a clinically diagnosed menstrual disorder (e.g., polycystic ovarian syndrome or amenorrhea) (SG1/3)
  • premenstrual dysphoric disorder (PMDD) (SG1/3)
  • history of epileptic seizure
  • history of depression
  • history of manic or psychotic episode
  • existing/current eating disorders (bulimia nervosa, anorexia nervosa) within the past 5 years
  • currently or history of (regular) consumption of illegal drugs within the last year
  • known diseases of the cardiovascular system
  • arterial hypertension above 160/90 mmHg at rest
  • known pulmonary diseases
  • arthritis and rheumatic diseases and conditions
  • hematologic diseases
  • orthopedic or other diseases (e.g. neurological) that preclude maximum load on the bicycle ergometer

Lab values

  • anemia (\<12.0 g/dl for women and \<14.0 g/dl for men)

Other

  • SG3 and SG4: More than 1 hour moderate exercise per week
  • pregnancy or breastfeeding (SG1/3)
  • inability to communicate adequately in speech
  • inability to follow instructions
  • alcohol consumption as equivalent doses of more than 12 g of pure alcohol per day on average for women and 24 g of pure alcohol per day for men
  • vegan diet
  • daily nicotine consumption
  • bronchial asthma

Who the study is looking for

  • age: 18-40 years
  • BMI: between 18.5 and 24.9 kg/m2 (SG1/2) or BMI between 25.0 and 39.9 kg/m2 (SG3/4)
  • ability to understand the study procedure and give consent
  • Written informed consent
  • SG1 women: any fitness level
  • SG2 men: VO2max \< 45 ml/kg/KG29,30
  • Available to conduct CPET on menstrual cycle days 1-5 (SG1/3)
  • No infection with HIV or Hepatitis B/C

Age in the registry: 18 years to 40 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Zurich
Coordinator of this site? Confirm its status
ZurichSwitzerlandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.