An interventional study of Metacognitive therapy and work-focused interventions and Waiting list in Anxiety and Depression, sponsored by Norwegian University of Science and Technology. Status unknown at 1 site in Norway. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-09-19.
Sponsored by Norwegian University of Science and Technology · Not applicable, Interventional, and Treatment
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Among 109 studies in Depression with a site in Norway — 22 open to participants now, 31 under way, none of them phase 3. Depression · Norway.
Among the 109 studies in Depression with a site in Norway, this one is the 28th largest by planned enrollment of the 81 interventional ones that give a count, is one of 4 that started in 2017, is one of 66 with no phase, and was the 46th registered.
8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.
Browse Depression studies →22 of the 109 studies in Depression with a site in Norway are open now. Recruiting first, the newest first:
Sorlandet Hospital HF · Sites in Norway
Ages 16–25
University of Bergen · Sites in Norway
Ages 18–40 · Healthy volunteers
University Hospital of North Norway · Sites in Norway
Ages 18–65
Solli Distriktspsykiatriske Senter · Sites in Norway
Ages 18–65
Norwegian University of Science and Technology · Sites in Norway
Ages 18–65
A study can be open while its sites in Norway have not opened yet or have stopped. Only those recruiting at a site in Norway →
Of the 1,089 Depression studies recruiting now, 470 (43%) set no upper age limit and 519 (48%) stop at 75 or younger; 203 take children under 18; 311 take healthy volunteers.
This study: 18 Years and older · all sexes · healthy volunteers too.
The full table on the hub →This tab as a report to print or save as PDF → With an account.
109 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 1 3 · Phase 2 7 · Phase 3 4 · Phase 4 2
First in 2001; this study’s year is marked. 4 started in 2017.
By drug class, each counting the studies that test any of its medicines:
This study's planned enrollment of 240 is above the median of 81 across 7,066 interventional studies indexed under Depression.
Median enrollment 170 across the 81 interventional studies, 575 across the 28 observational. Of the 68 that completed or were terminated, 3 (4%) have results posted.
This tab as a report to print or save as PDF → With an account.
4 of 109 have an industry lead sponsor. The 10 most frequent:
Norwegian University of Science and Technology is the lead sponsor of 495 studies on the registry; 48 are open to participants now.
Norwegian University of Science and Technology has 8 studies filed under Depression — fewer than ten, so there is no comparison to draw.
8 of the studies in Depression with a site in Norway that are under way reach primary completion within a year, 0 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT05734547Norwegian Center for Violence and Traumatic Stress StudiesStepping Together for Children After Trauma, Norway | 2026-12-01 |
| NCT07864324University Hospital of North NorwayHigh-Intensity Interval Training and Mental Health in Psychiatric Inpatients | 2026-12-15 |
| NCT06777693NKS Olaviken Gerontopsychiatric HospitalThe Unified Protocol for Transdiagnostic Treatment of Emotional Disorders in Older Adults: a Feasibility Study | 2026-12-24 |
| NCT07000799University of OsloA Study of School Absenteeism and Student Well-being in Elementary Schools | 2026-12-31 |
| NCT06568419Solli Distriktspsykiatriske SentereBehandling - Health and Work for Patients in Specialist Mental Health Care | 2027-04 |
Add all 8 to your calendar (.ics) → With an account.
Among the 109 studies in Depression with a site in Norway, from their registry updates:
This tab as a report to print or save as PDF → With an account.
Common mental health disorders such as anxiety and depression are leading causes of sickness absence and disability in Norway. Despite tremendous costs for individual and society, effective treatment is lacking. Mental health interventions do not typically target work situation, despite its importance for patient well-being. On a policy level, effective measures are impeded by a paucity of scientific data, and programs designed to address the issue such as Faster Return to Work ("Raskere tilbake") lack evaluation. The present project will test the effectiveness of Metacognitive therapy and work-focused interventions for reducing sick leave in patients with common mental disorders.
Common mental health disorders (CMD) such as anxiety and depression are leading contributors to the global burden of disease , generating substantial costs for societies in reduced productivity and increased benefit pay outs. In 2010, the worldwide cost of mental health disability was estimated at US$2.5-8.5 trillion in lost output, and the sum is projected to double by 2030 unless effective policy measures are implemented. For middle- and high-income countries, 30-50 % of disability applications stem from mental health issues, and the proportion is likely greater among the younger part of the work force. In Europe, depression is responsible for 13.7 % of all years lived with disability, and anxiety disorders likely have similar impact. Mental health issues are among the leading causes of disability and early retirement across the European region.
For affected individuals, anxiety and depression reduces quality of life, decreases functioning and increases the risk of further health problems. Sick leave is often used for adults with CMD, but may not always be helpful. Avoidance and isolation are behavioural strategies that maintain anxiety and depression. Absenteeism from work, an important social arena, may strengthen this behaviour, impeding recovery. Even when controlling for the impact of ill health, short term sick leave may in itself increase the risk of future long term absence. In addition, employment rates are 10-15% lower for people with mental ill health than the rest of the population. Exclusion from the work force is in turn associated with poorer mental health, and can heighten the risk of futures depression and even suicide. The relationship between CMD and reduced work-participation is therefore likely bidirectional, and sick leave may not work as intended despite its high cost for society.
The individual and societal burden from sick leave and mental health represents a key policy challenge on the global agenda and the need for efficient measures is urgent. Norway exemplifies this urgent need as expenditure on disability and sickness absence totals 5 % of GDP, by far the highest in the OECD. Efforts have been made to address the issue through several policy initiatives, such as the nationwide Faster Return to Work (FRW) program. The program facilitates buying treatment from different actors to reduce waiting times and thus potentially the duration of sick leave. The impact of the program is uncertain, as little research has been done on its efficacy. Scientific data on Norwegian sick leave follow up is mostly absent. Despite the magnitude of the challenge, there is a clear knowledge gap.
Investment in sick leave follow up has not been equally distributed amongst patient groups. Sixty per cent of all working days lost to disability or sick leave are due to mental health issues and musculoskeletal complaints. Sick leave due to CMD is growing. When caused by mental health issues, disability pension is awarded on average nine years earlier than for somatic reasons, resulting in more working years lost to disability. Though prevalent in the statistics, few CMD patients on sick leave receive treatment. Only 1.4 % of employees on sick leave are referred to specialized mental health treatment. As many as one in three people awarded disability pension for mental illness have never received any form of treatment prior to disability being granted. This shows a severe under-referral and under-treatment for this patient group despite being responsible for the majority of sick leave and disability costs.
A more targeted approach, integrating work-focused interventions with effective CMD treatment is needed for this patient group. Two recent studies have examined such an approach. In the Netherlands, Lagerveld and Blonk conducted a randomized controlled trial where 168 patients on sick leave due to CMD received either cognitive behavioural therapy (CBT), or CBT with an integrated work-focused intervention. Their results showed a 20 % decrease in sickness absence for patients receiving the work-focused intervention, while maintaining effective symptom reduction. In Germany, similar results were found with a smaller sample size. A multicentre trial in Norway looked at registry data for 1193 CMD patients receiving a variation of work-specific interventions, showing a clear reduction in sick leave and disability. Integrated work-focused treatment for CMD is thus a promising avenue of research.
Metacognitive therapy (MCT) is a treatment based on more recent theoretical developments. It has shown excellent results for anxiety and depression, and the treatment protocol for generalized anxiety disorder and social phobia is recommended in the NICE guidelines. Rather than challenging and changing specific thought content (CBT), metacognitive treatment aims to change and challenge maladaptive cognitive processes, among these rumination and worry, which are key components in CMD and sick leave.
The study will be a randomized controlled trial. Participants will be persons with a primary diagnosis of common mental disorders, anxiety and depression. Experienced independent diagnosticians will assess all patients by using structural interviews MINI (MINI International Neuropsychiatric Interview).
All patients will be randomized in blocks to two groups in order to compare the following conditions: MCT and work-focused interventions, and a wait list control condition. After the waiting period of either 8 or 12 weeks, the patients in the wait-list condition will be allocated to the treatment condition. Both between-subjects and within-subjects comparisons will be conducted.
Questions that will be addressed are:
The meta-cognitive treatment program is based on Wells' manual. The work-focused intervention is based on an adopted Norwegian version of Lagerveld and Blonk. The interventions are run in parallel. The patients who are receiving MCT and work-focused interventions will be treated up to maximum 12 sessions, with weekly session of 45-60 minute duration.
The treatment will be administered according to the originators published treatment protocols for MCT.
Criteria for recovery will be: Jacobsen criteria of a minimum change and patients crossing the cut-off point on two measures: The BDI and BAI. Other outcome measures will include:
A comparison between the two groups of patients will be conducted at post-treatment. Follow-up data will be analysed based on 6 month and at one year of follow up for the treatment condition with self-report and a four year follow-up with register data. A within group analyses will be conducted in order to estimate effect sizes and significant clinical change estimates.
Participants will be randomized in patients divided on three conditions in a 1:2 ratio. One factors are controlled for in the randomization, namely, gender. A computer program provided by NTNU WebCRF will generate the randomization list.
8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.
This study's planned enrollment of 240 is above the median of 81 across 7,066 interventional studies indexed under Depression.
Browse Depression studies →Norwegian University of Science and Technology is the lead sponsor of 495 studies on the registry; 48 are open to participants now.
Compared within Depression, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Anxiety Disorders. The counts are of registry records indexed under each term, refreshed daily. How we classify →
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Clinically significant
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Work-focused metacognitive therapy
Behavioral: Metacognitive therapy and work-focused interventions
Waiting list
Behavioral: Metacognitive therapy and work-focused interventions · Other: Waiting list
Metacognitive therapy and work-focused interventions, up to maximum 12 sessions, with weekly session of 45-60 minute duration. The metacognitive treatment program is based on Wells' manual. The work-focused intervention is based on Lagerveld and Blonk. The interventions are run in parallel.
Waiting list
Changes in degree of sick leave
data from National registers
Time frame: From 2 years prior to intervention - to 4 years after intervention
Changes in degree of sick leave
data from patients self-report
Time frame: From 2 years prior to intervention - to 4 years after intervention
Changes in anxiety symptoms
Changes in depressive symptoms measured by Beck Anxiety Inventory (BAI)
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
Changes in depressive symptoms
Changes in depressive symptoms measured by Beck Depression Inventory II (BDI-II)
Time frame: From pre treatment, to post treatment (12 weeks), 6 months 1 year follow-up
Changes in metacognitions
Changes in metacognitions symptoms measured by the Metacognitions Questionnaire 30 (MCQ-30)
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
Changes in subjective health complaints
Changes in symptoms measured by Subjective Health Complaints
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
Changes in bullying and victimisation at work
Changes in measured Negative Acts Questionnaire
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
Changes in self-efficacy
Changes measured with Return to work self-efficacy
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
Changes in resilience
Changes measured with The resilience scale for adults (RSA)
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
Changes in quality of life
Changes measured with EQ-5D-5L
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
MINI - diagnostic interview
Diagnostic evaluations using MINI - International Neuropsychiatric Interview
Time frame: From pre treatment, to post treatment (12 weeks)
Secondary analysis related to the onset of Covid-19
Sub-analyses taking into consideration the onset of Covid-19 in Norway by mid March 2020
Time frame: From pre treatment, to post treatment (12 weeks), 6 months and 1 year follow-up
Plan to share: No
Started Oct 2017 (actual). Primary completion is estimated for Apr 2023, 66 months after the start.
Of 3,471 non-industry interventional studies with no phase under Depression, half reached primary completion within 21 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 41. This study's planned 66 months is above that.
Counting every sponsor, half of 3,569 studies reached it within 21 months; a quarter within 9 and three quarters within 41.
How these figures are worked out, and which studies are left out of them.
This study is status unknown, as verified in Sep 2022. You cannot join it, but the record below documents what was studied.
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Norwegian University of Science and Technology →