Impact of Depression on Thermoregulation

Last updated: January 30, 2026
Sponsor: Penn State University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Depression

Treatment

N/A

Clinical Study ID

NCT06805851
Study26326
  • Ages 18-40
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

The purpose of this study is to determine if, compared to non-depressed adults, differences exist in skin blood flow and sweating responses to passive heat stress in adults with clinically diagnosed depression, those with depression who are prescribed and taking SSRIs and those with depression who are prescribed and taking SNRIs.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Non-depressed adults aged 18-40 years;

  • OR adults aged 18-40 years with clinically diagnosed major depressive disorderaccording to DSM-V criteria not currently receiving antidepressant treatment;

  • OR adults aged 18-40 years with clinically diagnosed major depressive disorder withat least 2 weeks of treatment with a selective serotonin reuptake inhibitor;

  • OR aged 18-40 years adults with clinically diagnosed major depressive disorder withat least 2 weeks of treatment with a serotonin norepinephrine reuptake inhibitor;

  • All participants will be asymptomatic and no signs/symptoms of disease according tothe American College of Sports Medicine 10th edition Guidelines for Exercise Testingand Prescription (chest pain or pressure, dizziness, joint pain, and signs ofcardiovascular disease);

  • Systolic blood pressure 140 mmHg and diastolic pressure 90 mmHg at screening;

  • Non-diabetic

  • Not taking any other medications that might affect the physiological variables ofinterest (beta blockers, tricyclic antidepressants, antipyretics, diuretics, etc.);;

  • Between the 20th and 80th percentiles for sex- and age-appropriate VO2max accordingto the American College of Sports Medicine 10th edition Guidelines for ExerciseTesting and Prescription;

  • English proficiency;

  • Capable of providing informed consent.

Exclusion

Exclusion Criteria:

  • BMI > 35

  • Are pregnant or planning to become pregnant in the next 12 months;

  • Concurrently participate in another study involving physical activity or weightloss;

  • Plan to have surgery or relocate outside the area within the next year;

  • Medications that could alter cardiovascular or thermoregulatory responses toexercise (beta blockers, antipyretics, tricyclic antidepressants, diuretics, etc.);

  • Allergy to latex or adhesive;

  • Tobacco use;

  • Illegal/recreational drug use;

  • Exertional chest pain or musculoskeletal pain;

  • Contraindications to a maximal exercise test or an indication for early terminationof the exercise test according to the American College of Sports Medicine 10thedition Guidelines for Exercise Testing and Prescription;

  • Abnormal resting or exercise electrocardiogram (ECG);

  • Any bleeding disorders, gastric ulcers, allergies to NSAIDS, asthma, kidney/liverdisorders, and taking any other anticoagulants;

  • History of Crohn's disease, diverticulitis, or similar gastrointestinal disease;

  • Co-morbid psychiatric disorders (psychosis, schizophrenia, bipolar disorder, panicdisorder, obsessive compulsive disorder, etc.);

  • Active suicidal ideation (moderate or high suicidality);

  • Use of psychoactive or psychopharmacological drugs other than SSRI and SNRIs withinone year of participating.

Study Design

Total Participants: 64
Study Start date:
March 01, 2025
Estimated Completion Date:
January 30, 2027

Study Description

Four groups will be recruited to examine the impact of major depressive disorder and pharmaceutical treatments on thermoregulatory heat loss mechanisms. Adults without MDD, adults with MDD, adults with MDD currently prescribed and taking selective serotonin reuptake inhibitors as treatment, and adults with MDD currently prescribed and taking serotonin norepinephrine reuptake inhibitors as treatment will be recruited to completed a passive heat stress experiment. All subjects will sign an informed consent form and undergo a medical screening prior to participation. Each subject will complete 1 passive heat stress experiment in which body temperature will be using a water perfused suit. During passive heating, body temperature, skin blood flow, and local and whole-body sweat rates will be continuously measured and recorded to compare heat stress responses between groups.

Connect with a study center

  • Noll Laboratory

    University Park, Pennsylvania 16802
    United States

    Site Not Available

  • Noll Laboratory

    University Park 5216774, Pennsylvania 6254927 16802
    United States

    Active - Recruiting

Map preview placeholder

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.