Your session is about to expire
← Back to Search
Intensive Short-Term Dynamic Psychotherapy for Somatic Symptom Disorder
N/A
Waitlist Available
Led By Joel M Town, DClinPsy
Research Sponsored by Nova Scotia Health Authority
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 8
Awards & highlights
Study Summary
This trial is testing whether ISTDP, a type of therapy, is more effective than usual medical care for treating somatic symptom and related disorders.
Eligible Conditions
- Somatic Symptom Disorder
- Intensive Short Term Dynamic Psychotherapy
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ week 8
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 8
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Somatic Symptom Severity score using the SOMS-7 from baseline to week 8
Secondary outcome measures
Change in depression score using the Patient Health Questionnaire-depression scale (PHQ-9) from baseline to 8 weeks
Change on Inventory of Interpersonal Problems (IIP-32) from baseline to week 8
Change on Whiteley Index for Health Anxiety from baseline to week 8
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Intensive Short Term Dynamic Psychotherapy (ISTDP)Experimental Treatment1 Intervention
Group II: Medical Care As Usual (MCAU)Active Control2 Interventions
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Intensive Short-Term Dynamic Psychotherapy
2014
N/A
~40
Find a Location
Who is running the clinical trial?
Nova Scotia Health AuthorityLead Sponsor
258 Previous Clinical Trials
83,817 Total Patients Enrolled
Joel M Town, DClinPsyPrincipal InvestigatorCapital District Health Authority and Dalhousie University
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Share this study with friends
Copy Link
Messenger