Trial Investigating the Effect of Different Exercise Forms on Depression
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|ClinicalTrials.gov Identifier: NCT00103415|
Recruitment Status : Unknown
Verified February 2005 by Demostudiet.
Recruitment status was: Active, not recruiting
First Posted : February 9, 2005
Last Update Posted : July 13, 2006
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During one year, 5-8% of the population will suffer from major depression. Some of the key symptoms are loss of interest in daily activities, loss of energy and sleeping disturbances. The financial consequences of this disease is estimated to be more than 30 million pounds per year in Great Britain and USA alone. There is an increasing interest in the effect exercise has on depression. Smaller studies indicate that exercise is a good treatment for depression. This study will be a large scale randomized trial and will hopefully bring important knowledge on the effects exercise has on depression.
We will compare the effect endurance training, weight-lifting exercise and a control group has on depressive symptoms after 4 months training, twice a week.
|Condition or disease||Intervention/treatment||Phase|
|Depression||Behavioral: Endurance training Behavioral: Weight-lifting training||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Enrollment :||300 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||Randomized Clinical Trial Investigating the Effect of Different Exercise Forms on Depression|
|Study Start Date :||February 2005|
|Study Completion Date :||February 2007|
- Remission (<8 HAMD-17)
- Response (50% reduction of score on HAMD-17)
- Job situation
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|Ages Eligible for Study:||18 Years to 55 Years (Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Age: 18-55
- ICD-10 diagnoses F32.0, F32.1, F33.0, F33.1
- Speak fluent danish
- Not able to do exercise
- Drug/alcohol addict
- The patient already engages in more than one hour of weekly exercise.
- The patient has not been working the last 24 months due to depression.
- Suicidal behavior.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00103415
|Psychiatric department, Bispebjerg Hospital|
|Copenhagen, Denmark, 2400|
|Principal Investigator:||Merete Nordentoft, M.D, Ph.D.||Bispebjerg Hospital|
|Other Study ID Numbers:||
|First Posted:||February 9, 2005 Key Record Dates|
|Last Update Posted:||July 13, 2006|
|Last Verified:||February 2005|