Skip to content

Intensive Psychotherapy for Chronic Depression

The Effectiveness of Intensive Psychotherapy for Chronic Depression: A Naturalistic Comparison With Treatment-as-Usual

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05221567
Enrollment
280
Registered
2022-02-03
Start date
2012-01-01
Completion date
2017-12-31
Last updated
2022-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Depression, Persistent Depressive Disorder, Recurrent Major Depression

Brief summary

The study evaluates whether Intensive psychotherapy show superior effect on chronic depression over TAU

Detailed description

Background: Accumulating evidence indicates that intensive psychotherapy (i.e., greater number of treatment sessions per time unit) improves outcomes for patients with mental health problems. However, few studies have investigated whether patients with chronic depression (CD) benefit from treatment with higher intensity. The main purpose of this study is to investigate if intensive psychotherapy could improve treatment for patients with chronic depression (CD). The primary research question is whether two intensive psychodynamic inpatient treatments, affect phobia therapy (APT) and VITA, are superior to low intensity treatment (TAU) at completion of treatment. To indicate if a potential difference between intensive treatment and TAU is due to the intensity of the therapy, the study contrasts two therapies with similar intensity, but different theoretical rationales. Methods: 280 patients with CD are included in a naturalistic study. Patients are assessed at four time points; assessment, start of therapy, end of therapy and 1-year follow-up. Three comparisons are performed with patients matched across groups; Intensive treatment (APT + VITA) vs TAU during treatment, APT vs VITA during treatment and APT vs VITA during follow-up. The outcome measure is the BDI-II.

Interventions

BEHAVIORALPsychotherapy

Intensive psychotherapy (i.e., greater number of treatment sessions per time unit)

Sponsors

Modum Bad
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

Inclusion criteria will be liberal and similar to clinical practice criteria at the treatment site which includes patients with the characteristics of chronic depression (CD), thus including patients with * Persistent depressive disorder as defined by the diagnostic and statistical manual of mental disorders (DSM5) * Recurrent depressive disorder as defined by the International classification of diseases-10 (ICD-10)

Exclusion criteria

* Not having utilized reasonably available treatment in proximity to their residence * A psychotic disorder * Cluster A or B personality disorder * Bipolar disorder, * Ongoing substance abuse, * Physical brain disorder * Not having access to TAU while on the 12 week wait-list period.

Design outcomes

Primary

MeasureTime frameDescription
Change in Depressive symptomsPatients were assessed at four time points; assessment, start of therapy (12 weeks after assessment), end of therapy (24 weeks after assessment) and at 1-year follow-up (76 weeks after assessment).Beck depression inventory II (BDI-II) Self-report instrument for assessing severity of depression. 21 items are scored on Likert scale from 0 to 4 (range 0-63). Scores between 14 and 19 indicate mild depression, 20 to 28 indicate moderate depression, and above 29 indicate major depression.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026