Major DepressionDEMOIINCT00695552
The Effect of Exercise on Depressive Symptoms in Unmedicated Patients
A study testing Aerobic exercise and Low impact exercise in people with Major Depression, run by University of Copenhagen at 1 site in Denmark.
Trial summary
This trial investigates the biological effect of exercise training on depression. Participants will randomly be allocated to either a aerobic exercise group performing exercise on stationary bikes or a group performing low-impact exercise such as stretching exercises. Read more about this study
- Who is it for?
- Ages 18 to 60 yearsHealthy volunteers can take part
- Conditions the study is for
- Major Depression
- What is being tested?
- Aerobic exercise and Low impact exercise
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 115 participants
- Where
- 1 siteDenmark
- Study dates
- Sep 2008to Apr 2011
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 60 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- 18 - 60 years
- Major depression according to DSM-IV
- Living within 30 km of training facilities
- Able to read and understand informed consent
Who cannot join
- Recreational or current drug abuse
- Having used antidepressant medication within the last 2 months
- Contraindications to physical exercise
- Recreational exercise> 1 hour per week
- Medication for diabetes, hypertension, or any kidney disease
- Suicidal behaviour (ham-d17 item3 > 2)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: DEMO II: A Randomized, Parallel-group, Observer-blinded Clinical Trial of Aerobic Exercise Versus Stretching Exercise for Patients With Light to Moderate Depression
This trial investigates the biological effect of exercise training on depression. Participants will randomly be allocated to either a aerobic exercise group performing exercise on stationary bikes or a group performing low-impact exercise such as stretching exercises. Both groups will attend sessions three times per week for 3 months. Before and after the intervention the investigators will measure the severity of depression using the Hamilton depression rating scale (HAM-D17).
Read the detailed description
The yearly incidence of depression is estimated to be 3-5%, with a lifetime prevalence of 17% in western societies.Furthermore, Major depression is associated with increased mortality from somatic disorders such as cardiovascular disease, stroke, and endocrinological diseases. WHO and others stated that unipolar depressive disorders was the leading cause of disease burden in the western world in 2002 accounting for 9,0% of all disability adjusted life years. Projecting the current development in disease patterns unipolar depression is expected to be the second highest cause of global disease burden in 2030. With remission rates of approximately 50% using medical antidepressant therapy, the search for alternative or augmentation therapy is a key issue in depressive research.
In 2001 a meta-analysis concluded that the effect of exercise training could not be determined due to lack of good quality research. The authors found that the majority of trials were without blinded outcome assessment, lacked intention-to-treat analysis, and most had short follow-up. In this context, one of the authors in 2004 launched a pragmatic randomized controlled trial investigating the effect of exercise training on depressive symptoms - the DEMO trial(10). The 165 included participants were randomized to either aerobic, non-aerobic, or relaxation training in a four-month training programme. The primary outcome was the Hamilton depression rating scale (HAM-D17) and data collection ended June 1st 2007. After four month intervention there were no overall effect of exercise on depressive symptoms; the estimate at four month between non-aerobic and relaxation training was -0.9 (95%CI: -3.2 to 1.4) and between aerobic and relaxation training was 0.99 (95%CI: -1.3 to 3.3). These results do not support any biological effect of exercise on major depression. However, the majority (115/165) of patients had received antidepressant medication for more than six weeks at baseline thus the lack of a positive result could partly be explained by a treatment resistant group. A subgroup analysis of patients not medicated at baseline estimated the effect between non-aerobic and relaxation training to -1.7 (95% CI: -6.0 to 2.5) and between aerobic and relaxation training to 0.3 (95% CI: -3.9 to 4.6). The number of patients in this important sub-group, means that any conclusion on non-medicated patients is underpowered. In addition the literature suggest that the possible effect of exercise on depression is frequency and intensity related. In the DEMO trial the participants only trained twice pr. week.
This result from the DEMO trial is somewhat in contrast with the abundant publications of animal research showing that exercise stimulates hippocampal neurogenesis and in theory improves depressive symptoms and cognitive skills. The hippocampus is involved in cognitive functions such as memory and learning processes as well as regulation of the hypothalamus. In depression and neurodegenerative diseases such as Alzheimer and Parkinson Disease, which share features like impaired memory and learning abilities, the hippocampus is characterized by atrophia. In addition to a decreased hippocampal volume, brain imaging studies have observed reduction in volume of prefrontal cortex of depressed patients, though postmortem studies have less evident results.
Prospective studies on healthy adults suggest that exercise has a beneficial effect on cognitive functions or reduces an age related decline in these. Research on rodents suggest that an increase in memory and learning in relation to exercise is mediated through an up-regulation of brain derived neurotrophic factor, which has the ability to stimulate synaptic-plasticity.
Interestingly the exercise induced cell proliferation is inhibited by peripheral blockade of either insulin growth factor 1 (IGF-1) or vascular endothelial growth factor (VEGF), which could indicate that the exercise induced neurogenesis is dependent of IGF-I/VEGF. The role of IGF-I in neurogenesis is supported by studies showing an increase in new hippocampal cells in sedentary animals given IGF-I infusion. Fibroblast growth factor 2 (FGF-2) also increases in the rat hippocampus in response to exercise, however FGF-2 injections into the adult rat hippocampus do not increase neurogenesis. The importance of IGF-I in neurogenesis is emphasized by the fact that homozygous IGF1 -/- mice at the age of to months had reduced brain weight affecting all major brain areas, especially the volume of the dentate gyrus(33) in contrary to BDNF null mutant mice that did not show major hippocampal deficits.
Furthermore, it has been shown that antidepressant treatment up-regulates sBDNF in humans and a relationship between genetic variants of BDNF locus and depression have been implied. On this background it could be argued that low BDNF levels contribute to the pathophysiology of depression, and that exercise has a beneficial effect on cognitive function in patients with depression through an up-regulation of IGF-1, VEGF and BDNF.
The effect of exercise on hippocampal neurogenesis and cognition have recently been supported in a human study measuring cerebral blood volume in the dentate gyrus by magnetic resonance imaging.
On this background the investigators have designed this randomized trial comparing aerobic exercise and no treatment in light to moderate depression. This trial will employ adequate methods of reducing bias such as centralized randomization, blinded outcome assessment, and analysis according to the intent-to-treat principle. In addition the investigators plan to include a healthy control group to establish any differences in biological response to exercise
Objectives The primary objective for the DEMOII superiority trial is to assess the beneficial and harmful effect of aerobic exercise versus stretching exercise in patients diagnosed with moderate depression according to ICD-10. The primary outcome will be an assessment of depressive symptoms as measured with the Hamilton Depression Scale (HAM-D17), by outcome assessors blinded to intervention group.
The secondary objective is to measure the effect of exercise on neurogenesis in the hippocampal region by cerebral blood volume. The assessors will be blind to participation status.
Tertiary objects is to evaluate cognitive skills, brain derived neurotrophic factor, insulin like growth hormone 1, vascular endothelial growth factor, and other variables associated with the development of cardiovascular disease (interleukin 6, maximal oxygen uptake, BMI, tumour necroses factor alpha and blood pressure).
- Conditions
- Major Depression
- Being tested
- Aerobic exercise, Low impact exercise
- Keywords
- Major depression, exercise
- Medical subject headings
- Depressive Disorder, Major, Motor Activity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Aerobic exerciseBehavioural
Aerobic exercise on stationary bikes. Three sessions/week for 3 three months. First month the workload is equivalent to 65% of HRmax, the second month the workload is equivalent to 70% of HRmax, and the third month the workload is equivalent to 75% of HRmax
Low impact exerciseBehavioural
Participants meets 3 times/week for 3 months. They will engage in low impact activities such as stretching exercises
| Study group | Role | What they receive |
|---|---|---|
| 1 | Experimental | Aerobic exercise on stationary bikes. Three sessions/week for 3 three months. First month the workload is equivalent to 65% of HRmax, the second month the workload is equivalent to 70% of HRmax, and the third month the workload is equivalent to 75% of HRmax Receives: Behavioral: Aerobic exercise |
| 2 | Placebo comparator | Participants meets 3 times/week for 3 months. They will engage in low impact activities such as stretching exercises. Receives: Behavioral: Low impact exercise |
What is being measured
The primary outcome is the main question the study is designed to answer.
HAM-D17
Measured: Before and after 3 months intervention
Secondary outcomes (1)
Remission from depression (not fulfilling the DSM-IV criteria for depression and a hamilton rating below 8)
Measured: Before and after 3 months intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jun 2008 (estimated)
- Study startSep 2008
- Primary completionJan 2011
- Study completionApr 2011
Why it stopped: The recruitment process were slower than expected. Not enough money to continoue
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Major DepressionStudies of the same condition, open and under way.
- More trials run by University of CopenhagenThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 115 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Copenhagen
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Merete Nordentoft, Professor, DMSc., University of Copenhagen
- Investigators
- Jesper Krogh, M.D, Principal investigator, Psychiatric Center Bispebjerg, Bispebjerg University Hospital, Copenhagen Denmark
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00695552
- Sponsor's protocol ID
- DEMOII
- Acronym
- DEMOII
- Status last verified
- May 2023
- First submitted
- 10 Jun 2008
- Last updated
- 11 May 2023
- Results posted
- No
- Data monitoring committee
- No
Publications
Krogh J, Rostrup E, Thomsen C, Elfving B, Videbech P, Nordentoft M. The effect of exercise on hippocampal volume and neurotrophines in patients with major depression--a randomized clinical trial. J Affect Disord. 2014 Aug;165:24-30. doi: 10.1016/j.jad.2014.04.041. Epub 2014 Apr 23.
PubMed 24882173Krogh J, Videbech P, Thomsen C, Gluud C, Nordentoft M. DEMO-II trial. Aerobic exercise versus stretching exercise in patients with major depression-a randomised clinical trial. PLoS One. 2012;7(10):e48316. doi: 10.1371/journal.pone.0048316. Epub 2012 Oct 31.
PubMed 23118981
Study at a glance
From the registry record, last updated by the sponsor on 11 May 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- DEMO II: A Randomized, Parallel-group, Observer-blinded Clinical Trial of Aerobic Exercise Versus Stretching Exercise for Patients With Light to Moderate Depression
- ClinicalTrials.gov ID
- NCT00695552
- Acronym / sponsor ID
- DEMOII / DEMOII
- Conditions
- Major Depression
- Keywords
- Major depression, exercise
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: The recruitment process were slower than expected. Not enough money to continoue
- Enrolment
- 115 participants (actual)
- Lead sponsor
- University of CopenhagenUniversity, hospital or other
- Study start
- Sep 2008
- Primary completion
- Jan 2011 (actual)
- Study completion
- Apr 2011 (actual)
- First posted
- 12 Jun 2008 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This trial investigates the biological effect of exercise training on depression. Participants will randomly be allocated to either a aerobic exercise group performing exercise on stationary bikes or a group performing low-impact exercise such as stretching exercises. Both groups will attend sessions three times per week for 3 months. Before and after the intervention the investigators will measure the severity of depression using the Hamilton depression rating scale (HAM-D17).
Detailed description
The yearly incidence of depression is estimated to be 3-5%, with a lifetime prevalence of 17% in western societies.Furthermore, Major depression is associated with increased mortality from somatic disorders such as cardiovascular disease, stroke, and endocrinological diseases. WHO and others stated that unipolar depressive disorders was the leading cause of disease burden in the western world in 2002 accounting for 9,0% of all disability adjusted life years. Projecting the current development in disease patterns unipolar depression is expected to be the second highest cause of global disease burden in 2030. With remission rates of approximately 50% using medical antidepressant therapy, the search for alternative or augmentation therapy is a key issue in depressive research.
In 2001 a meta-analysis concluded that the effect of exercise training could not be determined due to lack of good quality research. The authors found that the majority of trials were without blinded outcome assessment, lacked intention-to-treat analysis, and most had short follow-up. In this context, one of the authors in 2004 launched a pragmatic randomized controlled trial investigating the effect of exercise training on depressive symptoms - the DEMO trial(10). The 165 included participants were randomized to either aerobic, non-aerobic, or relaxation training in a four-month training programme. The primary outcome was the Hamilton depression rating scale (HAM-D17) and data collection ended June 1st 2007. After four month intervention there were no overall effect of exercise on depressive symptoms; the estimate at four month between non-aerobic and relaxation training was -0.9 (95%CI: -3.2 to 1.4) and between aerobic and relaxation training was 0.99 (95%CI: -1.3 to 3.3). These results do not support any biological effect of exercise on major depression. However, the majority (115/165) of patients had received antidepressant medication for more than six weeks at baseline thus the lack of a positive result could partly be explained by a treatment resistant group. A subgroup analysis of patients not medicated at baseline estimated the effect between non-aerobic and relaxation training to -1.7 (95% CI: -6.0 to 2.5) and between aerobic and relaxation training to 0.3 (95% CI: -3.9 to 4.6). The number of patients in this important sub-group, means that any conclusion on non-medicated patients is underpowered. In addition the literature suggest that the possible effect of exercise on depression is frequency and intensity related. In the DEMO trial the participants only trained twice pr. week.
This result from the DEMO trial is somewhat in contrast with the abundant publications of animal research showing that exercise stimulates hippocampal neurogenesis and in theory improves depressive symptoms and cognitive skills. The hippocampus is involved in cognitive functions such as memory and learning processes as well as regulation of the hypothalamus. In depression and neurodegenerative diseases such as Alzheimer and Parkinson Disease, which share features like impaired memory and learning abilities, the hippocampus is characterized by atrophia. In addition to a decreased hippocampal volume, brain imaging studies have observed reduction in volume of prefrontal cortex of depressed patients, though postmortem studies have less evident results.
Prospective studies on healthy adults suggest that exercise has a beneficial effect on cognitive functions or reduces an age related decline in these. Research on rodents suggest that an increase in memory and learning in relation to exercise is mediated through an up-regulation of brain derived neurotrophic factor, which has the ability to stimulate synaptic-plasticity.
Interestingly the exercise induced cell proliferation is inhibited by peripheral blockade of either insulin growth factor 1 (IGF-1) or vascular endothelial growth factor (VEGF), which could indicate that the exercise induced neurogenesis is dependent of IGF-I/VEGF. The role of IGF-I in neurogenesis is supported by studies showing an increase in new hippocampal cells in sedentary animals given IGF-I infusion. Fibroblast growth factor 2 (FGF-2) also increases in the rat hippocampus in response to exercise, however FGF-2 injections into the adult rat hippocampus do not increase neurogenesis. The importance of IGF-I in neurogenesis is emphasized by the fact that homozygous IGF1 -/- mice at the age of to months had reduced brain weight affecting all major brain areas, especially the volume of the dentate gyrus(33) in contrary to BDNF null mutant mice that did not show major hippocampal deficits.
Furthermore, it has been shown that antidepressant treatment up-regulates sBDNF in humans and a relationship between genetic variants of BDNF locus and depression have been implied. On this background it could be argued that low BDNF levels contribute to the pathophysiology of depression, and that exercise has a beneficial effect on cognitive function in patients with depression through an up-regulation of IGF-1, VEGF and BDNF.
The effect of exercise on hippocampal neurogenesis and cognition have recently been supported in a human study measuring cerebral blood volume in the dentate gyrus by magnetic resonance imaging.
On this background the investigators have designed this randomized trial comparing aerobic exercise and no treatment in light to moderate depression. This trial will employ adequate methods of reducing bias such as centralized randomization, blinded outcome assessment, and analysis according to the intent-to-treat principle. In addition the investigators plan to include a healthy control group to establish any differences in biological response to exercise
Objectives The primary objective for the DEMOII superiority trial is to assess the beneficial and harmful effect of aerobic exercise versus stretching exercise in patients diagnosed with moderate depression according to ICD-10. The primary outcome will be an assessment of depressive symptoms as measured with the Hamilton Depression Scale (HAM-D17), by outcome assessors blinded to intervention group.
The secondary objective is to measure the effect of exercise on neurogenesis in the hippocampal region by cerebral blood volume. The assessors will be blind to participation status.
Tertiary objects is to evaluate cognitive skills, brain derived neurotrophic factor, insulin like growth hormone 1, vascular endothelial growth factor, and other variables associated with the development of cardiovascular disease (interleukin 6, maximal oxygen uptake, BMI, tumour necroses factor alpha and blood pressure).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 1 | Experimental | Behavioral: Aerobic exerciseAerobic exercise on stationary bikes. Three sessions/week for 3 three months. First month the workload is equivalent to 65% of HRmax, the second month the workload is equivalent to 70% of HRmax, and the third month the workload is equivalent to 75% of HRmax |
| 2 | Placebo comparator | Behavioral: Low impact exerciseParticipants meets 3 times/week for 3 months. They will engage in low impact activities such as stretching exercises. |
Who may qualify
- Ages
- 18 to 60 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- 18 - 60 years
- Major depression according to DSM-IV
- Living within 30 km of training facilities
- Able to read and understand informed consent
Key exclusion criteria (6 listed)
- Recreational or current drug abuse
- Having used antidepressant medication within the last 2 months
- Contraindications to physical exercise
- Recreational exercise> 1 hour per week
- Medication for diabetes, hypertension, or any kidney disease
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Aerobic exerciseAerobic exercise on stationary bikes. Three sessions/week for 3 three months. First month the workload is equivalent to 65% of HRmax, the second month the workload is equivalent to 70% of HRmax, and the third month the workload is equivalent to 75% of HRmax | Behavioural | 1 |
| Low impact exerciseParticipants meets 3 times/week for 3 months. They will engage in low impact activities such as stretching exercises | Behavioural | 2 |
Primary outcome
HAM-D17
Time frame: Before and after 3 months intervention
1 secondary outcome
Remission from depression (not fulfilling the DSM-IV criteria for depression and a hamilton rating below 8)
Time frame: Before and after 3 months intervention
Results and safety
The study was stopped early (reason given: The recruitment process were slower than expected. Not enough money to continoue). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 May 2023.
- Derived from this study: PubMed 24882173Krogh J, Rostrup E, Thomsen C, Elfving B, Videbech P, Nordentoft M. The effect of exercise on hippocampal volume and neurotrophines in patients with major depression--a randomized clinical trial. J Affect Disord. 2014 Aug;165:24-30. doi: 10.1016/j.jad.2014.04.041. Epub 2014 Apr 23.
- Derived from this study: PubMed 23118981Krogh J, Videbech P, Thomsen C, Gluud C, Nordentoft M. DEMO-II trial. Aerobic exercise versus stretching exercise in patients with major depression-a randomised clinical trial. PLoS One. 2012;7(10):e48316. doi: 10.1371/journal.pone.0048316. Epub 2012 Oct 31.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jesper Krogh, M.D principal investigator
Psychiatric Center Bispebjerg, Bispebjerg University Hospital, Copenhagen Denmark
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Aerobic exercise and Low impact exercise in people with Major Depression, run by University of Copenhagen at 1 site in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 11 May 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: The recruitment process were slower than expected. Not enough money to continoue). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
HAM-D17 (time frame: Before and after 3 months intervention). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00695552, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 May 2023.