Somatic Symptom Disorder Clinical Trial
Official title:
How Much Does the Therapist Matter in Internet Based Emotional Awareness and Expression Therapy (I-EAET) for Functional Somatic Disorder? A Randomised Controlled Trial of I-EAET With and Without Therapist Support
Verified date | March 2024 |
Source | Stockholm University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Functional somatic syndromes (e.g. irritable bowel syndrome, fibromyalgia) and medically unexplained symptoms (e.g. chronic primary pain) are very common in primary care. These patients make 14 times more doctor visits than the general population, but describe themselves as less satisfied with the care they receive. Although Region Stockholm in Sweden recently developed care flows based on 'step up' care for the most common patient groups in primary care, patients with functional or medically unexplained symptoms are not mentioned. Short-term psychodynamic therapies such as Emotional Awareness and Expression Therapy (EAET) and Intensive Short Term Psychodynamic Therapy (ISTDP) have recently been evaluated in three systematic reviews and show good results for patients with medically unexplained symptoms. Short-term psychodynamic therapy considers that good treatment outcomes for patients with functional somatic syndromes can be achieved by increasing awareness of emotions and teaching patients to better experience, express and regulate emotions. In several randomized studies, short-term psychodynamic therapy has shown good effects even compared to other treatments, including cognitive behavioral therapy (CBT). The overall purpose of this research project is to to evaluate psychodynamic emotion-focused interventions (EAET and ISTDP) for patients with medically unexplained symptoms/functional somatic symptoms (MUS/FSD). The project includes several studies that will clarify effects and contribute to information on how care flows in primary care for the patient group can be created. The research question for this specific study is: Is internet-based Emotional Awareness and Expression Therapy (I-EAET) with therapist more effective than without therapist support for patients with FSD?
Status | Recruiting |
Enrollment | 150 |
Est. completion date | December 31, 2025 |
Est. primary completion date | June 1, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - The research subject certifies that he/she has undergone medical assessment for his/her physical symptoms. - The subject rates either moderate distress from bodily symptoms in the PHQ-15 (over 10 points) or severe distress from a single bodily symptom (at least 2 points for this symptom). - The research participants expresses interest in investigating whether emotional factors such as stress may contribute to symptoms. - Research subjects either affirm the presence of emotionally difficult life events (affirm at least 1 such event in the Adverse Childhood Experience (ACE-10) or reach the proposed cut-off point of 23p in the PCL-5). - Drugs used should have been stable for at least 1 month. Exclusion Criteria: - Research subjects suffer from ongoing substance abuse (alcohol or drugs) or are deemed to have serious mental illness (psychotic illness, suicidal ideation, antisocial personality disorder etc). - The research subjects have ongoing medication of a clearly addictive and sedative nature (e.g. benzodiazepines). - The research subject participates in other psychological treatment focusing on physical symptoms. However, other psychological treatment is allowed where the support therapy does not take place more often than once a month. - The research subject does not master the Swedish language sufficiently to be able to assimilate written material in Swedish. |
Country | Name | City | State |
---|---|---|---|
Sweden | Stockholm University | Stockholm | |
Sweden | Stockholm University | Stockholm |
Lead Sponsor | Collaborator |
---|---|
Daniel Maroti | Wayne State University |
Sweden,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Mediational measure: DERS-16 | Ratings on emotional (dys)regulation. Higher scores indicates worse symptom/functioning. | Each week once a week throughout 10 weeks of treatment | |
Other | Mediational measure: PHQ-15 | Ratings 0-2 on how troublesome somatic symptoms are experienced. Higher scores indicates worse symptom/functioning. | Each week once a week throughout 10 weeks of treatment | |
Other | Mediational measure: PHQ-4 | Ratings 0-2 on how troublesome somatic symptoms are experienced. Higher scores indicates worse symptom/functioning. | Each week once a week throughout 10 weeks of treatment | |
Primary | Patient Health Questionnaire -15 (PHQ-15) | Ratings 0-2 on how troublesome somatic symptoms are experienced. Higher scores indicates worse symptom/functioning. | Change from pre to post treatment (after 10 weeks of treatment) | |
Primary | Numeric Rating Scales according to EURONET-SOMA | Visual analogue scale 0-10 for symptom intensity and symptom interference. Higher scores indicates worse symptom/functioning. | Change from pre to post treatment (after 10 weeks of treatment) | |
Secondary | Generalized Anxiety Disorder-7 (GAD-7) | Ratings 0-3 on impact of anxiety symptoms. Higher scores indicates worse symptom/functioning. | Change from pre to post treatment (after 10 weeks of treatment) | |
Secondary | Patient Health Questionnaire-9 (PHQ-9) | Ratings 0-3 on impact of depressive symptoms. Higher scores indicates worse symptom/functioning. | Change from pre to post treatment (after 10 weeks of treatment) | |
Secondary | Post traumatic stress disorder checklist-5 (PCL-5) | Ratings 0-4 on impact of post traumatic symptoms. Higher scores indicates worse symptom/functioning. | Change from pre to post treatment (after 10 weeks of treatment) | |
Secondary | Difficulties in Emotion Regulation Scale-16 (DERS-16) | Ratings on emotional (dys)regulation. Higher scores indicates worse symptom/functioning. | Change from pre to post treatment (after 10 weeks of treatment) | |
Secondary | Sheehan Disability Scale (SDS) | Visual analogue scale 0-10 for symptom interference in daily life. Higher scores indicates worse symptom/functioning. | Change from pre to post treatment (after 10 weeks of treatment) | |
Secondary | The revised illness perception questionnaire (IPQ-R) | Ratings on illness beliefs. | Change from pre to post treatment (after 10 weeks of treatment) |
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