Exercise for Depression (EXDEP)
Depression, Unipolar, Bipolar Disorder
About this trial
This is an interventional treatment trial for Depression, Unipolar focused on measuring Depression, Unipolar depression, Bipolar affective disorder, Exercise, Internet-based intervention
Eligibility Criteria
Inclusion Criteria:
- Ability to understand the purpose and risks of the study and provide signed and dated informed consent and authorization to use confidential health information in accordance with national and local subject privacy regulations.
- Aged 18 to 65 years old, inclusive, at the time of informed consent.
- Montral Cognitive Assessment (MoCA) > 26 to exclude cognitive impairment.
- Apart from a clinical diagnosis of major depression or bipolar affective disorder, the subject must be in good health as determined by the Investigator, based on medical history and physical examination.
- QIDS scores > 5
Exclusion Criteria:
- Use of antidepressive medications or benzodiazepines at doses that have not been stable for at least 6 weeks prior to Screening
- Psychotherapy that started less than 8 weeks prior to Screening
- Any clinically significant psychiatric illness other than major depression or bipolar affective disorder
- Transient ischemic attack or stroke or any unexplained loss of consciousness within 1 year prior to Screening
- Any uncontrolled medical or neurological/neurodegenerative condition that, in the opinion of the Investigator, might impair treatment compliance and adherence
- History of unstable angina, myocardial infarction, chronic heart failure (New York Heart Association Class III or IV), or clinically significant conduction abnormalities (e.g., unstable atrial fibrillation) within 1 year prior to Screening
- Clinically significant 12-lead ECG abnormalities, as determined by the Investigator
- Uncontrolled hypertension defined as: average of 3 systolic blood pressure [SBP]/diastolic blood pressure [DBP] readings > 165/100 mmHg at Screening
History of malignancy or carcinoma, with the following exceptions:
i) Subjects with cancers in remission more than 5 years prior to Screening. ii) Subjects with a history of excised or treated basal cell or squamous carcinoma. iii) Subjects with prostate cancer in situ.
- History of seizure within 2 years prior to Screening.
- Recent history (within 1 year of Screening) of alcohol or substance abuse as determined by the Investigator, a positive urine drug (due to non-prescription drug) or alcohol test at Screening
- Clinically significant systemic illness or serious infection (e.g., pneumonia, septicemia) within 30 days prior to or during Screening
- History of human immunodeficiency virus (HIV), hepatitis C virus (HCV) or hepatitis B virus (HBV)
- Any other medical conditions (e.g., renal disease) that are not stable or controlled, or, which in the opinion of the Investigator, could affect the subject's safety or interfere with the study assessments
- Female subjects who are pregnant or currently breastfeeding
- Participation in another study
- Other unspecified reasons that, in the opinion of the Investigator or Biogen, make the subject unsuitable for enrollment
Sites / Locations
- Department of Psychiatry and Psychotherapy, University Medical Center, Mainz
- Department of Sports Medicine, Johannes Gutenberg University, Mainz
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Exercise Group
Treatment as usual group
Experimental arm type will assess whether a newly developed, supervised 8-week individualized, internet-based exercise therapy is effective in reducing depressive symptoms.
Treatment as usual. Other form of therapy (e.g. antidepressive medication) will not be affected.