Center for Psychiatry Research
Stockholm, Sweden
Location status: Recruiting
NCT Number: NCT06105502
The project is a longitudinal observation study that aims to systematically evaluate selected parts of the material collected within the framework of the psychotherapy training conducted at the Center of Psychotherapy Education and Research unit at Karolinska Institutet and Region Stockholm, Sweden. Students at the unit, patients being administered psychotherapy by the students, and supervisors will participate in the study.
The aim of the present study is to investigate the associations between (1) content and quality of psychotherapy supervision, (2) student therapists' competence, and (3) patient outcomes following student-led psychotherapy.
Interested in participating?
Request InfoAll sexes
Observational
Stockholm, Sweden
Location status: Recruiting
The project is a longitudinal observation study that aims to systematically evaluate selected parts of the material collected within the framework of the psychotherapy training conducted at the Center of Psychotherapy Education and Research unit at Karolinska Institutet and Region Stockholm, Sweden, from 2023 - 2028. The courses/programs that will be included in the project are the psychotherapist program (six semesters), the specialist training for psychologists in adult psychiatry (six semesters), the basic training in evidence-based psychotherapeutic methods (three semesters), and the basic training in psychotherapy for residents in child, adolescent, and adult psychiatry (two semesters). The element of the programs that will be evaluated is student-led psychotherapy, in which students conduct psychotherapy with patients in the public health care system.
The study's research subjects are supervisors, students, and their patients from the unit's student-led psychotherapies. Data consists of material that the supervisors and students have collected within the framework of the educational setting; the data are placed and stored on a secure digital platform (BASS). For objective estimates, the project also intends to code selected audio-recorded psychotherapy and supervision sessions.
The primary research questions are:
The project also aims to psychometrically evaluate (validity and reliability) some of the included instruments.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Psychotherapy education, including supervision, lectures, and workshops
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The GAD-7 is originally a measure for generalized anxiety disorder, but it is also frequently used to assess general anxiety. The form consists of seven items with a four-point scale. The range is 0-21 points. An eight item describes how disruptive the anxiety is from not at all to very significant, which is not included in the total score. The GAD-7 has been translated into Swedish and has shown good psychometric properties in terms of both reliability and validity.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The PHQ-9 is a well-established depression questionnaire consisting of nine items that correspond to the diagnostic criteria for a major depressive episode according to the DMS-5. How often the symptoms have bothered the patient in the past two weeks is rated by the patient, at the start and end of treatment, on a four-point scale. The range is 0-27 points. The PHQ-9 has been translated into Swedish and has good internal consistency and test-retest reliability.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The WHODAS 2.0 is a widely used generic assessment instrument that provides a standardized method for measuring health and disability across cultures. The form is based on a set of questions from the International Classification of Functioning, Disability, and Health (ICF) that are sufficiently reliable and sensitive to measure changes after interventions. The form is available in seven different versions with 36 questions, 12 questions, and 12+24 questions as interview-administered, self-administered, and proxy-administered, respectively. In the project, the self-administered 12-question form is used.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy for those patients scoring above the cut-off at pre-treatment
The AUDIT is a widely used instrument for identifying hazardous and harmful alcohol consumption. The instrument was initially developed by the WHO and consists of a ten-item questionnaire designed to measure three domains: consumption, dependence, and alcohol-related harm. The project uses a cut-off point of 5 points as an indication of mild alcohol use disorder. The project uses the AUDIT-C, which includes the first three questions of the AUDIT.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The SCI will be used to measure sleep disorders. The SCI contains eight questions regarding nocturnal symptoms, function, performance, duration, frequency, and severity. The form is translated into Swedish, and the psychometric properties have been shown in studies to be acceptable to good.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The LSAS-SR is only used for patients with social anxiety disorder or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The PDSS-SR is only used for patients with panic disorder or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The PSWQ is only used for patients with generalized anxiety disorder or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The PCL-5 is only used for patients with posttraumatic stress disorder or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The OCI-R is only used for patients with obsessive-compulsive disorder or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The PSS-10 is only used for patients with stress or burnout problems or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The SHAI-14 is only used for patients with health anxiety problems or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The EDE-Q is only used for patients with eating disorders or similar.
Time frame: Change from pre-treatment to immediately after the end of psychotherapy
The DUDIT is only used for patients with drug problems or similar.
Time frame: Student and patient data immediately after the end of psychotherapy
At the end of each treatment, all students write a summary of the treatment consisting of questions about the student (socio-demographic and contextual), the patient (socio-demographic and clinical), and the treatment (e.g., content, duration, and compliance). The summary concludes by summarizing the results of the patient's pre- and post-measurements, which are guided by the patient's problem domain.
Time frame: At first session, first treatment session, fifth treatment session, and last treatment session
The CTS-R is a standard instrument for assessing CBT competence that measures both general psychotherapy aspects and specific CBT aspects. The instrument contains twelve items, which are rated on a scale from 0 to 6 points corresponding to six different categories of therapist competence (incompetent, novice, advanced, beginner, competent, knowledgeable, and expert). The CTS-R has been translated into Swedish and has shown acceptable psychometric properties in several studies.
Time frame: At first session, first treatment session, fifth treatment session, and last treatment session
The Short-SAGE is an observational tool to evaluate supervisors' skills and adherence to CBT supervision. Short-SAGE describes 14 behaviors (competencies of the supervisor and supervisee), grouped on two main factors: the Supervisor's set (specific behaviors of the supervisor that are believed to facilitate optimal learning through experience) and the Supervisee's set (specific learning competencies that can be observed in the supervisee). The assessor observes a tutoring session and rates the competencies observed on a 7-point scale. For training purposes, a simpler 3-point scale is used. The instrument is available in Swedish and English, is fairly new, and has only undergone preliminary psychometric evaluations.
Time frame: At first session, first treatment session, fifth treatment session, and last treatment session
The ESSA-19 is a behavioral coding system to evaluate supervisors' skills and adherence to MI supervision. ESSA has been developed to be used as a tool for structured feedback to MI supervisors and as a measure of supervisory integrity in clinical trials. The manual has been developed at the unit 2019. The instrument is relatively new and has only undergone preliminary psychometric evaluations.
Time frame: At the middle of the student term (week 10 out of 20)
A unit-developed set of 10 questions focusing on how the students perceive the supervisor and the supervision setting, e.g., regarding feedback, skills training, and activity.
Contact information is provided by the study sponsor or research team.
Maria Beckman, PhD
CONTACT
Markus Jansson-Fröjmark, PhD
CONTACT
Region Stockholm
Other Gov
Systematic Evaluation of Psychotherapy Training: Impact of Supervision and Training on Student Learning and Patient Outcomes
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07010991
Student, Student Education
Istanbul, Kavacık Beykoz, Turkey (Türkiye)
View Trial DetailsNCT06890325
Comprehensive Geriatric Assessment, Frailty
Vic, Barcelona, Spain
View Trial DetailsNCT07560228
Student Education
View Trial DetailsNCT07541248
Clinical Reasoning, Physiotherapy and Rehabilitation
View Trial Details