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Psychological Treatment for Paraphilic Disorders - Trial NCT06404684

Access comprehensive clinical trial information for NCT06404684 through Pure Global AI's free database. This phase not specified trial is sponsored by Region Stockholm and is currently Not yet recruiting. The study focuses on Paraphilic Disorders. Target enrollment is 14 participants.

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NCT06404684
Not yet recruiting
behavioral
Trial Details
ClinicalTrials.gov โ€ข NCT06404684
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Psychological Treatment for Paraphilic Disorders
Paraphilic Disorders and Other Conditions With Risk for Sexual Violence: the Evaluation of an Adapted Cognitive Behavioral Therapy (CBT) Manual for Paraphilic Disorders

Study Focus

Paraphilic Disorders

Cognitive behavioral therapy (CBT)

Interventional

behavioral

Sponsor & Location

Region Stockholm

Stockholm, Sweden

Timeline & Enrollment

N/A

Oct 01, 2024

Jan 01, 2028

14 participants

Primary Outcome

Questions about sexual behaviors (diary),Questions about sexual behaviors (diary),Frotteuristic Disorder:Current Assessment Scale (FD: CAS),Voyeuristic Disorder: Current Assessment Scale (VD: CAS),Exhibitionistic Disorder: Current Assessment Scale (ED: CAS),,Coercive Sexual Sadism Disorder: Current Assessment Scale (CSSD: CAS)

Summary

The goal of this randomized study is to learn if a psychological intervention can treat
 help-seeking patients with paraphilic disorders.
 
 The main questions it aims to answer are:
 
 1. Is psychological therapy helpful for the reduction of problematic sexual behaviors among
 patients with paraphilic disorders?
 
 2. Is psychological helpful for the reduction of psychiatric symptoms and risk factors for
 sexual violence and improving quality of life among patients with paraphilic disorders?
 
 3. How do patients with paraphilic disorders describe pathways to care (e.g. perceived
 obstacles to seeking care) and how do they experience the treatment?
 
 The treatment addresses specific sexual problems. It also addresses mental symptoms (e.g.
 depression and anxiety). A psychologist provides the treatment face to face (on site or
 video). The aim is to finish the treatment within 12 weeks.
 
 The patient will report symptoms on a daily basis. The patient will also be interviewed after
 completion of treatment. The investigator will pose questions such as Was there anything
 that was experienced as particularly helpful in the treatment?, Was there anything that was
 not helpful?. The investigator will also ask about treatment seeking behavior with questions
 such as What kinds of resources would be helpful if they were available?

ICD-10 Classifications

Neurosyphilis, unspecified
Other and unspecified syphilis
Symptomatic neurosyphilis
Other specified disorders of penis
Syphilis, unspecified

Data Source

ClinicalTrials.gov

NCT06404684

Non-Device Trial