ClinicalTrials.gg
Status unknownNCT03301922Updated Sep 19, 2022

Metacognitive Therapy and Work Interventions for Patients on Sick Leave Due to Common Mental Disorders

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.

Primary conditionDepressionRegistry: Anxiety DisordersReclassifiedWhy we changed it
Registry
Anxiety Disorders — the first condition term the registry derived for this study.
ClinicalTrials.gg
Depression
Why
  1. The registry often attaches Anxiety Disorders to studies about something else, and this study's title and listed conditions do not name it.
  2. The study's listed conditions name Depression.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Norwegian University of Science and Technology · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2022), so the status shown — last known as Recruiting — may be out of date.

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Phase
Not applicable
Study type
Interventional
Enrollment
240
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

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.

Planned enrollment
28th of 81
240 · median 170
Started
2017
with 3 others
No phase
66 of 109
16 open now
Registered
46th of 109
by date
Lead sponsor
7 of 109
Norwegian University of Science and Technology

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.

Depression

8,582 studies on the registry are indexed under Depression; 1,723 are open to participants now.

Browse Depression studies →

Open to participants now

22 of the 109 studies in Depression with a site in Norway are open now. Recruiting first, the newest first:

17 more — sign in →

All 22 open studies →

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 →

Who these studies take

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.

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 109 studies in Depression with a site in Norway, or all of them as a file.
02

Study summary

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.

Read the detailed description

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:

  1. MCT and work-focused interventions will be superior to the wait-list condition in make participants return to work
  2. Which changes in predictors related to treatment predict return to work
  3. MCT and work-focused interventions will be superior to the wait-list condition for improving mental health
  4. MCT and work-focused interventions will be more cost-efficient than the wait-list condition
  5. Evaluate the sustainability of return to work for patients on sick leave due to common mental disorders after MCT and work-focused interventions
  6. Examine impact of different potential prognostic factors on work function, both at the end of treatment and at one year follow-up.
  7. If the effect of MCT and work-focused interventions will sustain one year after the end of therapy
  8. Explore if patients will have reduced use of sick leave in the four years following after treatment compared to the two years prior to treatment based on register data.

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.

  1. All patients referred to the clinic will be consecutively assessed at intake (MINI). Based on diagnosis and criteria for inclusion and exclusion, the patients will be asked to volunteer to participate in the study and confirm by signing a form of consent.
  2. Patients will be randomized to one of the two conditions.
  3. Patients will be asked to self-rate symptoms on a battery of self-report questionnaires.
  4. Work-focused meta-cognitive therapy will be given to patients in group 1, while group 2 is a waiting list control. Waiting list controls will be rated but not treated and will wait for treatment for either 8 or 12 weeks.
  5. After waiting they will be transferred to the treatment group.
  6. The patients will be assessed prior to treatment, by at end of treatment weeks in treatment, and at six months and at, one and two years of follow-up.
  7. Reassessment of the diagnosis and symptom severity is made by post-treatment.

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:

  • Reduction of depressive symptoms as measured by self-report questionnaires
  • Number of patients with no diagnosis based on MINI after treatment
  • Relapse rate during six months and at, one year follow-up

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.

03

Conditions studied

  • Anxiety
  • Depression

Browse trials for

Keywords

  • Occupational Health Services
  • Metacognitive therapy
  • Work focused interventions
  • Sick leave
04

In context

Depression Reclassified

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 →

Lead sponsor

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 →

05

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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.

Inclusion criteria

  • on sick leave either partial or full, due to
  • level of anxiety and depression, and
  • eligible for work-related sick leave pay outs
  • given consent

Exclusion criteria

Exclusion Criteria:

  • Serious mental illness (such as bipolar disorder or schizophrenia)
  • Substance abuse
  • Cluster A and B personality disorder
Terms in these criteria, in plain language(1)

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.

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.

06

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
240 participants (estimated)

Study arms

  • Experimental
    Work-focused metacognitive therapy

    Work-focused metacognitive therapy

    Behavioral: Metacognitive therapy and work-focused interventions

  • Other
    Waiting list

    Waiting list

    Behavioral: Metacognitive therapy and work-focused interventions · Other: Waiting list

Interventions

  • BehavioralMetacognitive therapy and work-focused interventions

    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.

  • OtherWaiting list

    Waiting list

07

What researchers measure

Primary outcomes

  1. Changes in degree of sick leave

    data from National registers

    Time frame: From 2 years prior to intervention - to 4 years after intervention

  2. Changes in degree of sick leave

    data from patients self-report

    Time frame: From 2 years prior to intervention - to 4 years after intervention

  3. 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

  4. 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

Secondary outcomes

  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. MINI - diagnostic interview

    Diagnostic evaluations using MINI - International Neuropsychiatric Interview

    Time frame: From pre treatment, to post treatment (12 weeks)

Other outcomes

  1. 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

08

Study locations

1 of 1 sites recruiting
  • Poliklinikken Raskere Tilbake, Diakonhjemmet Sykehus
    Oslo, Norway
    Recruiting
09

References and documents

Publications

  • Sandin K, Gjengedal RGH, Osnes K, Hannisdal M, Berge T, Leversen JSR, Rov LG, Reme SE, Lagerveld S, Blonk R, Nordahl HM, Shields G, Wells A, Hjemdal O. Metacognitive therapy and work-focused interventions for patients on sick leave due to anxiety and depression: study protocol for a randomised controlled wait-list trial. Trials. 2021 Nov 27;22(1):854. doi: 10.1186/s13063-021-05822-4. Erratum In: Trials. 2021 Dec 19;22(1):941. doi: 10.1186/s13063-021-05933-y. PubMed 34838125 ↗

Individual participant data

Plan to share: No

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

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.

Registered
Sep 29, 2017
First posted
Oct 4, 2017
StartActual
Oct 31, 2017
Primary completionEst.
Apr 2023
CompletionEst.
Apr 2023
Last update
Sep 19, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 19, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03301922
Collaborators
Diakonhjemmet Hospital
Responsible party
Sponsor
First posted
Oct 4, 2017
Start date
Oct 31, 2017
Primary completion
Apr 2023 (estimated)
Completion
Apr 2023 (estimated)
Last update
Sep 19, 2022

Study contacts

Odin Hjemdal, prof
Contact
odin.hjemdal@ntnu.no
0047 73597889
Odin Hjemdal, prof
principal investigator · Norwegian University of Science and Technology
Ragne GH Gjengedal
study chair · Diakonhjemmet Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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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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