CRACK-TARGET 1: ÉTUDE DESCRIPTIVE DE LA SENSIBILISATION COMPORTEMENTALE OBSERVÉE et ATTENTES

Cocaine Use Disorder Clinical Trial

— CRACK-TARGET  

Official title:

Descriptive Study of Observed Behavioural Awareness and Patients Expectations of Treatment

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06050304
• Other study ID #: 2022-A02072-41
• Status: Not yet recruiting
• Start date: September 2023
• Est. completion date: September 2024

Study information

• Verified date: August 2023
• Source: Assistance Publique - Hôpitaux de Paris
• Contact: Florence Vorspan, MD, PhD
• Phone: 01 40 05 44 17
• Email: Florence.vorspan[@]aphp.fr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This research focuses on behavioral sensitization (BS) a specific behavioural disturbance in crack-cocaine addiction. The primary objective is to observe whether BS can be demonstrated in an ecological setting in crack dependent users by continuous actimetry for 3 weeks. It is planned to include 20 persons with a current crack-cocaine addiction with a preferential use of rapid administration route (intravenous or smoke), in a care institution: Fernand Widal Hospital. In the proposed research, the investigators will assess the movements of crack-cocaine dependent users in relation to consumption. They will have to wear continuously for 3 weeks an actimeter. They will also have 3 blood tests trying to identify biomarkers of BS.

Description:

Paris region and the French west indies face a specific epidemic of crack-cocaine use, mostly by socially deprived subjects, highly visible in open drug scenes, with little access to the care system. Patients who suffer from crack-cocaine dependence experiment a high rate of medical and a high mortality rate, because this type of cocaine is a short-acting form, used through rapid route of administration (usually smoked or injected). Nevertheless, despite important uncovered medical needs, they are not often included in clinical trials and there is to date no pharmacological treatment for this severe condition. The investigators identified behavioral disturbances as a key problem in crack-cocaine dependence, as it is the second cause for emergency visits for those patients and a reason to be excluded from addiction care facilities. Based on preliminary results already gathered by our group, the investigators suggest that behavioral sensitization (BS), an increase of motor response to cocaine after repetitive intermittent use, could be assessed in Humans. Our goal is therefore to include 20 persons (10 males - 10 females) with a current cocaine use disorder,specifically crack users, with preferential use of rapid administration route (intravenous or smoke), in a care institution: the Fernand Widal Hospital (Assistance Publique - Hôpitaux de Paris). The investigators will assess the movements of crack-cocaine dependent users in relation to consumption. They will have to wear continuously for 3 weeks an actimeter, in the form of a small watch, which collects the level of motor activity throughout the day and night. They will be asked to indicate each moment of crack-cocaine use by pressing the button in the center of the watch. The investigators want to know if certain uses lead to more behavioral problems (especially after periods of cessation). They will also have 3 blood tests: the investigators want to know if blood proteins, genetic markers passed on by paricipants parents or the expression of proteins in particular situations, could predict this increase in motor effects for small doses of crack-cocaine. The investigators also want to better understand the needs of crack-cocaine dependent patients towards treatments and their expectations for recovery, by conducting a qualitative study where patients will participate in the definition of treatment aims to increase the efficiency of care With the project CRACK-TARGET 1 : DETA, the investigators aim at demonstrating the existence of BS in patients with crack dependent subjects. Furthermore, the investigators aim at developing specific, repeatable, easy to access measure of BS using questionnaires and objective actigraphy biomarkers to be used as surrogate endpoints in clinical trials.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: September 2024
• Est. primary completion date: September 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• > 18 years
• Have a current crack-cocaine use disorder defined as Severe Intensity Use Disorder (6 or more DSM5 criteria), AND preferential use of rapid administration route (intravenous or smoked)
• Self-identified male or female (n=10 males, n=10 females)
• Negative pregnancy test for females and use of effective contraception
• Be affiliated with a social security plan (or PUMA or CSS or AME)
• Sign an informed consent and commit to a 3-week follow-up in the study
• Have a weight greater than 40 kg

Exclusion Criteria:

• • Patient with a psychiatric disorder or symptoms that are not currently stabilized
• Patient who is a minor or under protective supervision (curatorship or guardianship)
• Patient in care at the request of a judicial authority (therapeutic injunction, classification with orientation)
• Pregnant or breastfeeding women
• Patients who do not speak French or English sufficiently
• Patients weighing less than 40 kg

Related Conditions & MeSH terms

• Cocaine Use Disorder

Intervention

Behavioral:
• Observation of behavior and search of biomarkers with 3 blood tests.3 weeks wearing an actimeter
In the form of a small watch, which collects the level of motor activity throughout the day and night. Patients will be asked to indicate each moment of crack-cocaine use by pressing the button in the center of the watch. We want to know if certain uses lead to more behavioral problems (especially after periods of cessation).

Biological:
• 3 blood tests
We will try to identify biomarkers of BS: blood proteins, genetic markers passed on by your parents, or the expression of proteins in particular situations

Locations

Country	Name	City	State
France	Hôpital Fernand Widal	Paris

Sponsors (2)

Lead Sponsor	Collaborator
Assistance Publique - Hôpitaux de Paris	Institut National de la Santé Et de la Recherche Médicale, France

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	A/G % in rs7568970 polymorphism of the LRP1B gene in patients with observed versus without observed BS	Fold change of the methylation status of the LRP1B gene in patients with observed versus without observed BS	3 weeks
Primary	Reduction in sleep duration(hours/minutes) on crack-cocaine use days following a break of at least 2 days compared to crack-cocaine use days without any break (means over the 3 weeks period)	Reduction in sleep duration(hours/minutes) on crack-cocaine use days following a break of at least 2 days compared to crack-cocaine use days without any break (means over the 3 weeks period)	3 Weeks
Secondary	Earlier onset of M10(the time of day when the 10 hours of peak motor activity begins, a reflection of the "motor wake-up time).	The time of day when the 10 hours of peak motor activity begins, a reflection of the "motor wake-up time") (hours/minutes) during crack-cocaine use days following a 2 days break compared to crack-cocaine use days without any break (comparison of mean M10 time)	3 Weeks
Secondary	Shorter relative amplitude of motor activity (the relative difference between M10)	Average activity level during the most active 10-hour period) and L5 (average activity level during the least active 5-hour period) (hours/minutes) during crack-cocaine use days following a 2 days break compared to crack-cocaine use days without any break (comparison of mean relative amplitudes over 3 weeks	3 Weeks
Secondary	Self-defined patients' expectations toward treatment measured in qualitative interviews	Expectations toward treatment measured in qualitative interviews	3 Weeks
Secondary	Higher scores assessed with questionnaires that approximate BS	Higher scores assessed with questionnaires that approximate BS	3 weeks
Secondary	WURS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	WURS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	3 weeks
Secondary	ASRS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	ASRS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	3 weeks
Secondary	SAPS-CIP in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	SAPS-CIP in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	3 weeks
Secondary	YMRS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	YMRS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	3 weeks
Secondary	UPPS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	UPPS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	3 weeks
Secondary	PDI in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	PDI in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	3 weeks
Secondary	PANSS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	PANSS in patients presenting with at least 1 of the 3 previously defition of BS on actimetric measures compared to patients without BS	3 weeks