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A Multiple Case Study of Schema Therapy for Difficult-to-treat Depression- DEPRE-ST*Case

A Multiple Case Study of Schema Therapy for Difficult-to-treat Depression - DEPRE-ST*Case

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06655623
Enrollment
3
Registered
2024-10-23
Start date
2024-11-06
Completion date
2026-12-19
Last updated
2025-09-23

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

Conditions

Depression, Major Depressive Disorder, Chronic Depression, Treatment Resistant Depression

Keywords

schema therapy, psychotherapy, difficult-to-treat depression

Brief summary

This clinical multiple case study seeks to expand the knowledge of how schema therapy could function as an intervention for difficult-to-treat depression. The study will explore in depth the course of a 30 session treatment with schema therapy conducted over approximately one year on three individual patients at two different psychiatric treatment sites. Together, the data from this study will inform about the feasibility of schema therapy for difficult-to-treat depression as well as form the base for recommendations in adapting schema therapy for this particular patient group.

Detailed description

The study is part of a larger randomized controlled study, the DEPRE-ST study (clinicaltrials.gov registration: NCT05833087)(Arendt et al., 2024). The study participants will also be part of the large trial, and will be recruited for the current case study when their randomization status is being revealed; i.e., they are randomized to schema therapy. In addition to the data collected in the DEPRE-ST trial, the patients will for each session self-report depression symptoms (before the session) and two different evaluations of the session (after the session). In addition, the patients' level of the schema therapy construct of 'Healthy Adult Mode' will be measured by self-report once monthly. And finally, the therapist will be interviewed at the end of the treatment course about important aspects of the content and outcome of the therapy. Video recordings of each session will provide detailed information about these aspects and the interventions used in therapy. The most important focus for the publication for this study will be to describe the trajectories of therapy for the participants, including content, effect, and subjective evaluations of therapists and participants. Also, the feasibility and adaptability of schema therapy for difficult-to-treat depression will be evaluated. Data from outcome measurements will be presented descriptively only. Interview and video data will be compared with the outcomes measurements to reveal important events and how they might be reflected in the replies to post-session evaluation questionnaires (Session Evaluation Questionnaire and Helpful Aspects of Therapy), and in the course of the participant's self-reported depression symptoms and Healthy Adult mode.

Interventions

BEHAVIORALSchema therapy

Schema therapy is a form of psychotherapy invented to address more complex clinical cases. It consists of elements from Cognitive Behavioral Therapy as well as psychodynamic, emotion-focused and gestalt therapies, with a distinct focus on experiential interventions. A therapy manual was developed for use in this study.

Sponsors

Mental Health Services in the Capital Region, Denmark
CollaboratorOTHER
Region of Southern Denmark
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Masking description

The participant and investigator are both blinded to condition at the initial baseline measurements, since randomization and assignment to treatment are only made after the baseline measurements have taken place.

Intervention model description

This study is a multiple case study of three patients with difficult-to-treat depression. The patients are also part of a larger, randomized controlled trial with two treatment arms (which also includes a Treatment As Usual arm), in which they have been assigned to the schema therapy arm.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Participants have at the time of inclusion been referred to treatment for depression as a primary diagnosis in a psychiatric clinic * Participants should meet the diagnosis of chronic or treatment-resistant depression as follows: 1. Clinical major depression as measured by the M.I.N.I. diagnostic interview: duration minimum two years OR persistent after = 2 trials of antidepressants from different classes, in an adequate dosage and time period (= 4 weeks) OR moderate treatment resistance as measured on the MSM-scale, score \> 6 2. Minimum a score of 9 points on the Hamilton Rating Scale for Depression 6 (HAMD-6), corresponding to moderate to severe depression

Exclusion criteria

* Alcohol or substance abuse * Bipolar or psychotic disorder * Acute suicidal risk * Mental disability (estimated IQ \< 70) * Non-Danish speaker * Known to be pregnant at time of inclusion Psychiatric comorbidity is not an

Design outcomes

Primary

MeasureTime frameDescription
Depression symptoms, as measured with the Hamilton Depression Rating Scale 6 items (HAMD-6), self-reportApproximately once a week during the course of therapy (30-52 weeks in total), before each therapy session (30 sessions in total)This scale was derived from the Hamilton Depression Rating Scale 17 items and focuses on the six core symptoms of depression.

Secondary

MeasureTime frameDescription
Patient's experience of helpful events in therapy, as measured by the Helpful Aspects of Therapy (HAT)Administered from the initiation of therapy, after every session (approximately once a week for 30-52 weeks, 30 sessions in total)The HAT was developed as a mixed qualitative and quantitative measure for describing what events in therapy were helpful or hindering for a good therapy outcome (Llewyn et al., 1988). This study will only include the first two items, which provide two blank text boxes for free writing of replies. The questions are: 1. Of the events which occurred in this session, which one do you feel was the most helpful or important for you personally? (By event we mean something that happened in the session. It might be something you said or did, or something your therapist said or did.) 2. Please describe what made this event helpful/important and what you got out of it.
Patient's experiences of important aspects of the therapy session and the patient's mood in relation to the session, as measured by the Session Evaluation QuestionnaireAdministered from the initiation of therapy, after every therapy session (approximately once a week, 30 sessions)The SEQ quantitively evaluates the psychotherapy session (9 items) and the patient's mood after the session (8 items)(the original SEQ was 21 items, but four items were removed for this study due to redundancy (Stiles et al., 1994)). Each item is scored on a bipolar, 7-point Likert scale, ranging from 1-7 and containing different, opposing aspects, e.g., 'bad-good', 'difficult-easy'. The patient is instructed to circle the appropriate number according to how they feel about the session and in themselves.
Healthy Adult schema mode, as measured on the Schema Schema Mode Inventory (SMI) - Healthy Adult subscaleAdministered from the initiation of therapy - once a month, i.e. 10-12 times in total, at the end of a session of schema therapy.The SMI was invented to measure the psychological construct of schema modes, which are emotional activations to the activation of inherent early maladaptive schemas (cognitive constructs mostly formed in childhood)(Lobbestael et al., 2010)Reiss et al., 2016). This study will only measure the Healthy Adult mode, as the strengthening of this mode is usually an important treatment focus in schema therapy. The Healthy Adult mode is measured in 10 items, containing different aspects of Healthy Adult, measured on a 6 point Likert scale ranging from 'Never or almost never' to 'Always'.

Other

MeasureTime frameDescription
Psychological well-being as measured on the WHO-5 Well-Being Index at 12 months after baseline measurementsFrom baseline measurements to 12 months after baseline measurements5-item questionnaire
Personal recovery after mental illness as measured on the INSPIRE-O Brief at 6 months after baseline measurementsFrom baseline measurements to 6 months after baseline measurements5-item questionnaire
Personal recovery after mental illness as measured on the INSPIRE-O Brief at 12 months after baseline measurementsFrom baseline measurements to 12 months after baseline measurements5-item questionnaire
Reactions to anger as measured on the Dimensions of Anger Reactions - Revised (DAR at 6 months after baseline measurementsFrom baseline measurements to 6 months after baseline measurements7-item questionnaire
Reactions to anger as measured on the Dimensions of Anger Reactions - Revised (DAR at 12 months after baseline measurementsFrom baseline measurements to 12 months after baseline measurements7-item questionnaire
Changes in anger processing as measured on the Metacognitive Anger Processing scale Short Version (MAP) at 6 months after baseline assessmentsFrom baseline measurements to 6 months after baseline measurements9-item questionnaire
Changes in repetitive negative thinking as measured on the Perseverative Thinking Questionnaire (PTQ) at 6 months after baseline assessmentsFrom baseline measurements to 6 months after baseline measurements15-item questionnaire
Changes in repetitive negative thinking as measured on the Perseverative Thinking Questionnaire (PTQ) at 12 months after baseline assessmentsFrom baseline measurements to 12 months after baseline measurements15-item questionnaire
Negative effects of treatment as measured on the Negative Effects Questionnaire (NEQ) at 6 months after randomizationFrom baseline measurements to 12 months after baseline measurements20-item questionnaire
Negative effects of treatment as measured on the Negative Effects Questionnaire (NEQ) at 12 months after randomizationFrom baseline measurements to 12 months after baseline measurements20-item questionnaire
Changes in 1-2 patient defined problems as measured on the Psychological Outcome Profiles (PSYCHLOPS) at 6 months after baseline assessmentsFrom baseline measurements to 6 months after baseline measurementsQuestionnaire with qualitative definition of patient defined problems and change on 6-point Likert scale
Changes in anger processing as measured on the Metacognitive Anger Processing scale Short Version (MAP) at 12 months after baseline assessmentsFrom baseline measurements to 12 months after baseline measurements9-item questionnaire
anxiety symptoms as measured on the Symptom Checklist-10 (SCL-10) at 6 months after baseline assessmentsFrom baseline measurements to 6 months after baseline measurements5-item questionnaire - only anxiety items are used
anxiety symptoms as measured on the Symptom Checklist-10 (SCL-10) at 12 months after baseline assessmentsFrom baseline measurements to 12 months after baseline measurements5-item questionnaire - only anxiety items are used
Changes in health-related quality of life as measured on the Euro-Qol-5D (EQ-5D) at 6 months after baseline assessmentsFrom baseline measurements to 6 months after baseline measurements5-item questionnaire
Changes in health-related quality of life as measured on the Euro-Qol-5D (EQ-5D) at 12 months after baseline assessmentsFrom baseline measurements to 12 months after baseline measurements5-item questionnaire
Prediction for treatment effect of negative expectancies for change in depression symptoms as measured on the Depression Change Expectancy Scale-pessimistic (DCES-P) items at baseline assessmentsAt baseline only11-item questionnaire - items about pessimistic expectations only
Schema modes as mediators of treatment effect after 6 months, as measured on the Schema Mode Inventory (SMI)From baseline measurements to 6 months after baseline measurements37-item questionnaire - a subset of the original 118-item measure, encompassing Vulnerable Child, Healthy Adult, Demanding Critic and Punitive Critic modes
Schema modes as mediators of treatment effect after 12 months, as measured on the Schema Mode Inventory (SMI)From baseline measurements to 12 months after baseline measurements118-item questionnaire
Early maladaptive schemas as measured after 6 months on the Young Schema Questionnaire 3 Short Form (YSQ-S3)From baseline measurements to 6 months after baseline measurements25-item questionnaire - a subset of the original 90-item measure, encompassing the schemas Emotional Deprivation, Abandonment, Mistrust/Abuse, Social Isolation, and Defectiveness
Early maladaptive schemas as measured after 12 months on the Young Schema Questionnaire 3 Short Form (YSQ-S3)From baseline measurements to 12 months after baseline measurements90-item questionnaire
Treatments for depression in earlier and current depressive episodeCollected at baseline onlyPsychotherapeutic, psychopharmacological treatment, Electroconvulsive therapy and psychiatric hospitalization, both collected from participant's given information and electronic journal records.
Childhood adversity, as measured on the Childhood Trauma Questionnaire (CTQ)Collected at baseline only28-item questionnaire
Changes in 1-2 patient defined problems as measured on the Psychological Outcome Profiles (PSYCHLOPS) at 12 months after baseline assessmentsFrom baseline measurements to 12 months after baseline measurementsQuestionnaire with qualitative definition of patient defined problems and change on 6-point Likert scale
Subjective functional impairment as measured on the Work and Social Adjustment Scale (WSAS) at 6 months after baseline measurementsFrom baseline measurements to 6 months after baseline measurements5-item questionnaire
Subjective functional impairment as measured on the Work and Social Adjustment Scale (WSAS) at 12 months after baseline measurementsFrom baseline measurements to 12 months after baseline measurements5-item questionnaire
Psychological well-being as measured on the WHO-5 Well-Being Index at 6 months after baseline measurementsFrom baseline measurements to 6 months after baseline measurements5-item questionnaire

Countries

Denmark

Contacts

Primary ContactStine B. Moeller, PhD
stinebm@health.sdu.dk+4551553898
Backup ContactIda-Marie TP Arendt, PhD-student
imarendt@health.sdu.dk+4551909649

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026