Dysthymia: Associated Costs, Treatment and Change Process

NCT ID: NCT04911829

Last Updated: 2021-06-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-01-31

Study Completion Date

2026-12-31

Brief Summary

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The study evaluates cost and effect of inpatient versus outpatient treatment of dysthymia, as well as investigates the processes through which psychotherapy works in treating dysthymia.

Detailed Description

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Inpatient treatment allows a more intensive treatment and allows the patient to be in a context where it is possible to focus on the processes in therapy with minimal interruption. Outpatient treatment is much less intensive but allows the treatment process to unfold in the context where the patient is experiencing the problems that brought them to therapy. It is not clear which of the contexts will be more effective in alleviating symptoms of dysthymia. Further, as dysthymia is a very costly disease for society it is of interest to know if the two treatments are cost-effective, and which one is the most cost effective.

A great paucity on dysthymia research ha left the psychotherapy field without an understanding of the processes through which dysthymia is changed. This study will investigate the change process through frequent assessments of common factors, psychological processes, symptoms, heart rate variability and cognitive attention bias.

Conditions

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Depression Cost Benefit Analysis Psychotherapeutic Processes

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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Inpatient treatment

High intensity high dosage inpatient short-term psychodynamic psychotherapy

Group Type ACTIVE_COMPARATOR

Psychotherapy

Intervention Type BEHAVIORAL

Outpatient treatment

Low dosage outpatient short-term psychodynamic psychotherapy

Group Type EXPERIMENTAL

Psychotherapy

Intervention Type BEHAVIORAL

Interventions

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Psychotherapy

Intervention Type BEHAVIORAL

Eligibility Criteria

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Exclusion Criteria

* current suicidal risk, current psychosis, marked emotional instability (i.e. issues with impulsivity), strong paranoid traits, current problems related to heavy substance abuse.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Modum Bad

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pål Ulvenes, PhD

Role: PRINCIPAL_INVESTIGATOR

Modum Bad

Locations

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Modum Bad

Vikersund, Buskerud, Norway

Site Status RECRUITING

Countries

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Norway

Central Contacts

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Pål Ulvenes, PhD

Role: CONTACT

Linne Melsom, Cand.Psy

Role: CONTACT

Facility Contacts

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Pål G Ulvenes, PhD

Role: primary

Terje Tilden, PhD

Role: backup

Other Identifiers

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Depression Forefront

Identifier Type: -

Identifier Source: org_study_id

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