Depression, Anxiety Clinical Trial
Official title:
An Outreach Collaborative Model for Early Identification and Treatment of Mental Disorder in Danish Workplaces
NCT number | NCT03786328 |
Other study ID # | 2013-18 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | April 1, 2008 |
Est. completion date | August 31, 2013 |
Verified date | December 2018 |
Source | Aalborg Universitetshospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Depression and anxiety are prevalent mental disorders among the working population with
potentially high personal and financial cost. The aim of the study is to test the
applicability of an outreach collaborative model for early identification and treatment of
clinical and sub-clinical mental disorders among Danish employees. applicability was examined
by I) investigating the fractions of identified and treated clinical and subclinical cases,
II) describing the distribution and characteristics of cases identified and III)
investigating the effect of allocated treatment.
A longitudinal study design with four assessments over 16 months are applied. Six
medium-large companies will be included, both public and private cooperations. Self-reporting
questionnaires probing for psychopathology will be distributed to all employees in the six
consecutively enrolled companies at the four time points. Employees meeting the screening
criteria at T1 will be assessed diagnostically. Subjects diagnosed with a clinical mental
disorder will be allocated to outpatient psychiatric treatment, and subjects with subclinical
conditions will be allocated to preventive cognitive behavioural therapy. Follow-up is
conducted 6 and 12 months after initiation of treatment.
Participation in the study is voluntary at all levels. Written informed consent will be
obtained from participant selected for diagnostic interview and treatment.
Status | Completed |
Enrollment | 73 |
Est. completion date | August 31, 2013 |
Est. primary completion date | August 31, 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion criteria: Individuals for the diagnostic interview and treatment are selected on the basis of their response to the SCL-90-R questionnaire. Hence, individuals are included in diagnostic interview, if scores on the SCL90-R inventory one of the following criteria: - Global Severity Index score > 0.63 or - values of > 0.63 in two or more subscales or - values of > 0.63 in the Depression subscale Exclusion criteria: - Individuals not meeting the above screening criteria will not participate in diagnostic interview and treatment |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Helle Østermark Sørensen | Spar Nord Foundation |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Severity of Psychopathological symptoms | The change in severity of psychopathological symptoms are measured with the Symptom Checklist 90, revised (SCL-90-R) that is a psychiatric self-report inventory with high reliability and validity to measure overall psychological distress and to detect changes. | Measured at baseline and 6 and 12 month follow-up |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04122482 -
An Online Course for Improving Knowledge and Access to Mental Health Accommodations in Canadian Enterprises
|
N/A | |
Completed |
NCT04085861 -
Mental Health in Dancers; an Intervention Study
|
N/A | |
Recruiting |
NCT06060210 -
Impact of Ketamine On Depressive Symptoms In Patients Undergoing Lumbo-peritoneal Shunt Insertion
|
Phase 4 | |
Active, not recruiting |
NCT04588883 -
Strengthening Families Living With HIV in Kenya
|
N/A | |
Recruiting |
NCT06065787 -
NeuroGlove Anxiety and Depression Study
|
N/A | |
Active, not recruiting |
NCT04583891 -
Mobile Apps to Reduce Distress in Breast Cancer Survivors Using an Adaptive Design
|
N/A | |
Completed |
NCT05554042 -
Kintsugi Voice Device Study
|
||
Not yet recruiting |
NCT06162624 -
Pilot Effectiveness Trial of an ACT Self-help Workbook Tailored Specifically for Prisons
|
N/A | |
Not yet recruiting |
NCT06430853 -
Psychobiological Interventions in Pregnancy
|
N/A | |
Completed |
NCT02954250 -
Mindfulness Based Cognitive Therapy for Depression and Cognitive Inhibition in Suicide
|
Early Phase 1 | |
Recruiting |
NCT05647499 -
Evaluating the Back 2 School Program in a Norwegian Setting: A Multicenter Pilot Study
|
N/A | |
Completed |
NCT03980873 -
Cognitive-Behavioral Therapy for Young Adult Lesbian, Gay and Bisexual: Transdiagnostic Minority Stress Approach
|
N/A | |
Completed |
NCT04422327 -
The Impact of a Combination of Bifidobacterium Longum 35624® and 1714™ Strains in Adults With Irritable Bowel Syndrome
|
Phase 1/Phase 2 | |
Completed |
NCT05368155 -
Chronic Pelvic Pain and Education Skills Training for Women Veterans
|
N/A | |
Completed |
NCT05455905 -
Voice Biomarkers Predictive of Depression and Anxiety
|
||
Completed |
NCT03272516 -
Mindfulness Based Cognitive Therapy (MBCT) for Primary Care Patients
|
N/A | |
Not yet recruiting |
NCT05493865 -
Parent-Child Single-Session Growth Mindset Intervention on Adolescent Depression and Anxiety Problems
|
N/A | |
Not yet recruiting |
NCT06027047 -
Breakthrough Anxiety and Sleep Evaluation Using Linked Devices and Smartphone Application Onar (BASEL)
|
||
Not yet recruiting |
NCT05535101 -
Non-invasive Brain Stimulation in Patients With Methamphetamine Use Disorder
|
N/A | |
Recruiting |
NCT04418115 -
Fatigue as a Late Effect in Breast Cancer Survivors - is Acupuncture a Treatment Option?
|
N/A |