Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:27 PM
Ignite Modification Date:
2025-12-24 @ 1:27 PM
NCT ID:
NCT01649895
Eligibility Criteria:
Inclusion Criteria:
* Outpatients
* Male or female
* ≥ 18 years
* Currently living in Stockholm, Uppland, Örebro, Södermanland, Gästrikland, Västmanland and Östergötland county in Sweden.
* Primary diagnosis of OCD according to the DSM-IV-TR.
* Signed informed consent
* Have regular access to a computer with internet access and skills to use the web
* Have received information about the need of using contraception
Exclusion Criteria:
* Pregnancy or breast feeding
* Patients unlikely to cooperate fully in the study
* Patients not able to read or understand the basics of the ICBT self-help material
* Psychotropic medication changes within two months prior to treatment
* Completed CBT for OCD within last 12 months
* Y-BOCS \[21\] \< 16 at Psychiatrist visit (6.2.3)pi
* OCD symptoms primarily associated with hoarding.
* Other primary axis I diagnosis according to the Mini-International Neuropsychiatric Interview (MINI) \[34\]
* Ongoing substance dependence
* Lifetime bipolar disorder or psychosis
* Suicidal ideation
* Axis II diagnosis that could jeopardize treatment participation
* Serious physical illness that will be an obstacle in ICBT and DCS
* Other ongoing psychological treatments that could affect OCD symptoms
* Epilepsia
* Renal impairment
* Hypersensitivity to D-Cycloserine
* Porphyria
* Chronic Alcoholism
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
100 Years
Study:
NCT01649895
Study Brief:
Protocol Section:
NCT01649895