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NCT Number: NCT06088732

Effects of Acute Exercise and Ibuprofen on Symptoms, Immunity, and Neural Circuits in Bipolar Depression

This is a 2x2, within-subjects, cross-over trial to test the anti-depressant effects of acute exercise in 20 participants with bipolar depression. Participants will complete four experimental sessions, two with an exercise challenge and two with a resting control condition in a counterbalanced order. Participants will receive either 800mg of ibuprofen or placebo before exercise or rest in order to test whether blocking the inflammatory response to exercise interferes with the neural and psychological effects of exercise.

Recruiting

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

Laureate Institute for Brain Research

Tulsa, Oklahoma, 74136, United States

Location status: Recruiting

Location contact

Jonathan Savitz, PhD

CONTACT

[email protected]

918-502-5104

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated informed consent form
  • Has an established residence and phone
  • Agrees to and is eligible for behavioral testing, magnetic resonance imaging, and blood draws.
  • Stated willingness to comply with all study procedures and lifestyle considerations (see Section 5.3, Lifestyle Considerations) and availability for the duration of the study
  • Males and females; Age 18-55 years
  • DSM-V diagnosis of bipolar disorder
  • Has a current major depressive episode
  • Depression at enrollment of sufficient severity to score > 11 on the QIDS
  • Be stably medicated for at least 4 weeks (a non-medicated subject may be included in the study if judged to be appropriate in the medical/psychiatric opinion of the investigator)
  • BMI between 18.5 and 35

Exclusion criteria

  • Diagnosis of any other major psychiatric disorder such as schizoaffective disorder, schizophrenia, or current psychotic depression
  • A history of bipolar disorder with rapid cycling
  • Concurrent manic symptoms of sufficient severity to pose a substantial risk of the development of a manic episode (>19 on the YMRS)
  • Current drug or alcohol or substance use disorder moderate or severe, except nicotine (within 6 months for severe use disorder; 2 months for moderate use disorder)
  • Volunteers currently receiving more than 4 mood-relevant psychotropic medications in a daily regimen (since this may signify a more brittle or complex clinical state)
  • Taking any of the following medications: medications with significant interactions with ibuprofen; immune-modulating medications (e.g. oral steroids); regular use of NSAIDs (> 3 times per week)
  • Current or prior cardiac disease, cardiac arrhythmia (e.g. supraventricular tachycardia, atrial fibrillation, ventricular fibrillation), or history of cardiac ablation therapy
  • Unstable medical condition, including significant respiratory disease (e.g., asthma, reactive airway disease (i.e., exercise induced asthma), or chronic obstructive pulmonary disease (COPD)), liver disease, hypothyroidism (i.e., condition not adequately stabilized for 3 months), or other conditions likely to require hospitalization or with a life expectancy of < 6 months (e.g., cancer).
  • History of claustrophobia that would prevent participation in imaging scans
  • Actively suicidal, as defined by expressive ideation with a plan and intent for suicide or developing suicidal ideation that requires immediate medical or treatment intervention or a suicide attempt within the previous six months
  • Participants who endorse a history of moderate to severe traumatic brain injury (>30 min. loss of consciousness or >24 hours posttraumatic amnesia) or other neurocognitive disorder with evidence of neurological deficits
  • Inadequate understanding of English
  • Currently pregnant or breast-feeding; fecund women not using adequate contraceptive methods; plan to become pregnant within 12 months
  • Metal in the body (e.g. history of working as a sheet metal worker) or pacemaker which is a contra-indication to magnetic resonance imaging
  • Has epilepsy, a neuromuscular disorder, or tardive dyskinesia
  • Has a chronic infectious illness
  • Requires immediate hospitalization for psychiatric disorder
  • Requires medications for a general medical condition that contraindicate any study medication
  • Receiving or have received during the index episode vagus nerve stimulation, electroconvulsive therapy, transcranial magnetic stimulation, or other somatic treatments
  • Allergy to, or other medical contraindication to ibuprofen (e.g. stomach ulcers)
  • Symptoms of myalgic encephalomyelitis/chronic fatigue syndrome or "long-COVID".
  • Current use of medications or dietary supplements for weight or appetite control, whether prescribed or not
  • Ulcerative colitis, Crohn's disease or other autoimmune disorder (except treated hypothyroidism)
  • Activity restrictions that limit the subject's ability to engage in intense physical activity
  • Use of beta-blockers, calcium channel inhibitors, or other heart-modulating medications (e.g., amiodarone)
  • Clinically significant abnormality on EKG
  • Hypertension, hepatitis, renal dysfunction, and/or anemia of sufficient severity to pose a risk to the participant
  • Moderate or heavy smoker based on Fagerstrom
  • Resting heart rate >100 beats per minute, systolic blood pressure > 160 mmHg, diastolic blood pressure > 100 mmHg
  • Clinically significant screening laboratory abnormalities not covered above
  • Any reason not listed herein that would make participation in the study hazardous

Treatment and study plan

Exercise Session

Other

30 min cycling on bicycle ergometer at 60% peak power output

Ibuprofen 800 mg

Drug

A single oral dose of Ibuprofen

Rest

Other

Resting for 30 min in chair

Placebo

Drug

Matched placebo

Primary outcomes

  1. Inflammation

    Time frame: Difference between IL-6 at baseline and two hours post intervention

    Serum concentrations of interleukin 6 (IL-6)

  2. Neural Response to Reward Anticipation

    Time frame: One hour post intervention

    Percent Signal Change in Ventral Striatum During Monetary Incentive Delay

Secondary outcomes

  1. Neural Response to Reward Receipt

    Time frame: One hour post intervention

    Percent Signal Change in Ventral Striatum During Monetary Incentive Delay (MID) task

  2. Brain Volume

    Time frame: One hour post intervention

    Gray Matter Volume of the Hippocampus

  3. Inflammation

    Time frame: Difference between TNF at baseline and two hours post intervention

    Serum concentrations of tumor necrosis factor (TNF)

  4. Inflammation

    Time frame: Difference between IL-10 at baseline and two hours post intervention

    Serum concentrations of interleukin 10 (IL-10)

  5. Anhedonia

    Time frame: Difference between SHAPS scores at baseline and two hours post intervention

    Score on the Snaith-Hamilton Pleasure Scale (SHAPS). Higher scores indicate greater anhedonia. Score range from 0-14.

Study contacts

Contact information is provided by the study sponsor or research team.

Jonathan Savitz

CONTACT

[email protected]

9185025104

Sponsors and collaborators

Lead sponsor

Laureate Institute for Brain Research, Inc.

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Oct 18, 2023
Registry last updated
May 23, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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