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Pilot Feasibility Study of Cognitive Control in Cocaine Dependence

Pilot Feasibility Study of Cognitive control in cocaine dependence: A multi-centre randomized controlled trial to pilot targeting craving for cocaine using memory reconsolidation techniques

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN16462783
Enrollment
30
Registered
2015-08-28
Start date
2015-06-01
Completion date
Unknown
Last updated
2023-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cocaine dependence Mental and Behavioural Disorders Cocaine dependence

Interventions

Informed, consenting adult participants will be randomised remotely by the Clinical Trials Unit Kings College, London to one of two conditions: Experimental Group: Experiment: Baseline cocaine cravi

Sponsors

Kings College London
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult (between 18 and 50 years old) 2. English speaking 3. Current diagnosis for cocaine dependence (ICD-10) 4. Self-reported regular cocaine use (weekly) and cocaine-positive UDS during screening 5. Motivation to reduce or quit cocaine use

Exclusion criteria

Exclusion criteria: 1. Current diagnosis of post-traumatic stress disorder (DSM-5) 2. Current non-medical benzodiazepine or harmful alcohol use (>50 units per week men; >35 units women) 3. Use of heroin or cocaine in the 24 hours before first CRF session 4. Clinically significant on-going medical problems that might make participation unsafe 5. Acute housing instability 6. Uncontrolled serious psychiatric illness 7. Significant neuro-cognitive functioning (<18, Montreal Cognitive Assessment) 8. Pregnant or breast feeding 9. Current enrollment in an addiction treatment related clinical research study

Design outcomes

Primary

MeasureTime frame
Change in craving intensity. Measured using the craving experience questionnaire (CEQ-11), adapted for cocaine for this study, at weeks 1 and 4 post randomization.

Secondary

MeasureTime frame
1. Physiological parameters during the craving provocation and memory reconsolidation and cognitive restructuring sessions: pulse rate, heart rate variability, electrodermal activity and skin conductance response. Mean and peak values will be computed: Days 1 to 5 of the intervention period 2. Self-report of cocaine useis assessed using a modified time-line follow-back (calendar prompt) interview to record instances of cocaine use during the study at weeks 1, 4 and 12 post randomization 3. Urine toxicology screening (UDS). By instant result immunoassay device for cocaine metabolite (benzolyecgonine) and morphine (morphine 2000 assay) at weeks 1, 4 and 12 post randomization and days 1 to 5 of the intervention 4. Audio-visual recordings: On a voluntary basis, each CRF session will be audio and video recorded via CCTV at the CRF 5. Treatment retention is assessed by recording the number of experimental participants who complete the 5-day CRF programme

Countries

England, United Kingdom

Contacts

Public ContactGarry Stillwell
garry.stillwell@kcl.ac.uk+44 20 7848 0901

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 7, 2026