Nutritional Intervention for College Students With Depression
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study is for college students age 18 or older with mild to moderate depression. It tests how well students can follow a Mediterranean diet, either alone or with eating limited to certain hours each day. Researchers will track food, meal times, sleep, and mood to see how practical these plans and study steps are.
The goal of this clinical trial is to assess the feasibility of nutritional interventions in college students with depression. The main outcomes it aims to measure are: * Nutritional content, meal timing, and sleep patterns in college students with depression * Feasibility of nutritional interventions (Mediterranean Diet and Time-Restricted Eating + Mediterranean Diet) in college students with depression Researchers will compare two groups - Mediterranean Diet (Med-Diet) and Time-Restricted Eating + Mediterranean Diet (TRE + Med-Diet) - to assess adherence to the dietary interventions and overall feasibility of the study procedures. Participants will: * Complete a 2-week baseline logging diet, sleep, activity, and mood * Be randomized to Mediterranean Diet (Med-Diet) or Time-Restricted Eating + Med-Diet (TRE + Med-Diet) * Participate in dietary counseling with a registered dietitian during the 8-week intervention * Continue to log diet, wear an actigraphy device, and complete mood, sleep, and diet assessments throughout the intervention
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- You are age 18 or older and enrolled in college.
- You have mild to moderate symptoms of depression.
- You are getting treatment for depression or are willing to get treatment during the study.
- You are generally in good physical health.
- Any medicine you take that affects weight, how your body uses energy, or mental health is at a steady dose.
Who can't join
- You have a higher risk of suicide.
- The study doctor decides you cannot take part safely.
- You have ever been diagnosed with bipolar disorder, schizophrenia, or post-traumatic stress disorder (PTSD). These conditions affect mood, thoughts, or responses to trauma.
- You currently have an eating disorder, such as bulimia, anorexia, or binge eating.
- You currently have an alcohol or drug use disorder.
- You have done shift work outside your class schedule in the past 30 days.
- You are pregnant or breastfeeding.
- You are receiving an experimental drug for depression or are in another study that requires you to change your diet.
Simplified for readability. The official criteria below are what the study team uses.
Official eligibility criteria
Inclusion Criteria: * Age ≥ 18 years and enrolled as a college student * Symptoms of mild to moderate depression * Receiving treatment for depression or willing to receive treatment during study participation * Generally in good physical health * On a stable dose of any medication affecting weight, metabolism, or mental health Exclusion Criteria: * Elevated risk for suicide * Inability to participate safely, as determined by the study physician * Lifetime diagnosis of bipolar disorder, schizophrenia, or post-traumatic stress disorder * Current eating disorder (e.g., bulimia, anorexia nervosa, binge eating) * Current alcohol or substance use disorder * Shift work outside of class schedule in the past 30 days * Pregnancy or lactation * Treatment with an investigational drug for depression or participation in another study requiring modification of diet
Study sites (1)
CA
- University of California San Diego · La Jolla, CA 92093Michael J McCarthy · Study contact · 858-534-8070 · mmccarthy@health.ucsd.eduMore trials in La Jolla