RECRUITING

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

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2024-03-12

Study Completion:2026-12-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06088732

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 55 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT

Inclusion Criteria	Exclusion Criteria
1. Provision of signed and dated informed consent form 2. Has an established residence and phone 3. Agrees to and is eligible for behavioral testing, magnetic resonance imaging, and blood draws. 4. 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 5. Males and females; Age 18-55 years 6. DSM-V diagnosis of bipolar disorder 7. Has a current major depressive episode 8. Depression at enrollment of sufficient severity to score \> 11 on the QIDS 9. 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) 10. BMI between 18.5 and 35	1. Diagnosis of any other major psychiatric disorder such as schizoaffective disorder, schizophrenia, or current psychotic depression 2. A history of bipolar disorder with rapid cycling 3. Concurrent manic symptoms of sufficient severity to pose a substantial risk of the development of a manic episode (\>19 on the YMRS) 4. 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) 5. 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) 6. 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) 7. Current or prior cardiac disease, cardiac arrhythmia (e.g. supraventricular tachycardia, atrial fibrillation, ventricular fibrillation), or history of cardiac ablation therapy 8. 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). 9. History of claustrophobia that would prevent participation in imaging scans 10. 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 11. 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 12. Inadequate understanding of English 13. Currently pregnant or breast-feeding; fecund women not using adequate contraceptive methods; plan to become pregnant within 12 months 14. 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 15. Has epilepsy, a neuromuscular disorder, or tardive dyskinesia 16. Has a chronic infectious illness 17. Requires immediate hospitalization for psychiatric disorder 18. Requires medications for a general medical condition that contraindicate any study medication 19. Receiving or have received during the index episode vagus nerve stimulation, electroconvulsive therapy, transcranial magnetic stimulation, or other somatic treatments 20. Allergy to, or other medical contraindication to ibuprofen (e.g. stomach ulcers) 21. Symptoms of myalgic encephalomyelitis/chronic fatigue syndrome or "long-COVID". 22. Current use of medications or dietary supplements for weight or appetite control, whether prescribed or not 23. Ulcerative colitis, Crohn's disease or other autoimmune disorder (except treated hypothyroidism) 24. Activity restrictions that limit the subject's ability to engage in intense physical activity 25. Use of beta-blockers, calcium channel inhibitors, or other heart-modulating medications (e.g., amiodarone) 26. Clinically significant abnormality on EKG 27. Hypertension, hepatitis, renal dysfunction, and/or anemia of sufficient severity to pose a risk to the participant 28. Moderate or heavy smoker based on Fagerstrom 29. Resting heart rate \>100 beats per minute, systolic blood pressure \> 160 mmHg, diastolic blood pressure \> 100 mmHg 30. Clinically significant screening laboratory abnormalities not covered above 31. Any reason not listed herein that would make participation in the study hazardous

Inclusion Criteria

Exclusion Criteria

1. Provision of signed and dated informed consent form
2. Has an established residence and phone
3. Agrees to and is eligible for behavioral testing, magnetic resonance imaging, and blood draws.
4. 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
5. Males and females; Age 18-55 years
6. DSM-V diagnosis of bipolar disorder
7. Has a current major depressive episode
8. Depression at enrollment of sufficient severity to score \> 11 on the QIDS
9. 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)
10. BMI between 18.5 and 35

1. Diagnosis of any other major psychiatric disorder such as schizoaffective disorder, schizophrenia, or current psychotic depression
2. A history of bipolar disorder with rapid cycling
3. Concurrent manic symptoms of sufficient severity to pose a substantial risk of the development of a manic episode (\>19 on the YMRS)
4. 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)
5. 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)
6. 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)
7. Current or prior cardiac disease, cardiac arrhythmia (e.g. supraventricular tachycardia, atrial fibrillation, ventricular fibrillation), or history of cardiac ablation therapy
8. 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).
9. History of claustrophobia that would prevent participation in imaging scans
10. 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
11. 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
12. Inadequate understanding of English
13. Currently pregnant or breast-feeding; fecund women not using adequate contraceptive methods; plan to become pregnant within 12 months
14. 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
15. Has epilepsy, a neuromuscular disorder, or tardive dyskinesia
16. Has a chronic infectious illness
17. Requires immediate hospitalization for psychiatric disorder
18. Requires medications for a general medical condition that contraindicate any study medication
19. Receiving or have received during the index episode vagus nerve stimulation, electroconvulsive therapy, transcranial magnetic stimulation, or other somatic treatments
20. Allergy to, or other medical contraindication to ibuprofen (e.g. stomach ulcers)
21. Symptoms of myalgic encephalomyelitis/chronic fatigue syndrome or "long-COVID".
22. Current use of medications or dietary supplements for weight or appetite control, whether prescribed or not
23. Ulcerative colitis, Crohn's disease or other autoimmune disorder (except treated hypothyroidism)
24. Activity restrictions that limit the subject's ability to engage in intense physical activity
25. Use of beta-blockers, calcium channel inhibitors, or other heart-modulating medications (e.g., amiodarone)
26. Clinically significant abnormality on EKG
27. Hypertension, hepatitis, renal dysfunction, and/or anemia of sufficient severity to pose a risk to the participant
28. Moderate or heavy smoker based on Fagerstrom
29. Resting heart rate \>100 beats per minute, systolic blood pressure \> 160 mmHg, diastolic blood pressure \> 100 mmHg
30. Clinically significant screening laboratory abnormalities not covered above
31. Any reason not listed herein that would make participation in the study hazardous

Contacts and Locations

Study Contact

Jonathan Savitz

CONTACT

9185025104

jsavitz@laureateinstitute.org

Study Locations (Sites)

Laureate Institute for Brain Research

Tulsa, Oklahoma, 74136

United States

Collaborators and Investigators

Sponsor: Laureate Institute for Brain Research, Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-03-12

Study Completion Date2026-12-31

Study Record Updates

Study Start Date2024-03-12

Study Completion Date2026-12-31

Terms related to this study

Additional Relevant MeSH Terms

Bipolar Depression