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NCT02308878 Clinical Trial

Mobile Health Cognitive Stimulation in Heroin Users

Substance Use Disorder Clinical Trial

— Re@dict  

Official title:
Executive Functioning in Heroin Users Following a Mobile Health Cognitive Stimulation Approach: a Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02308878
Other study ID # SLB_SUD01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2013
Est. completion date January 2020

Study information
Verified date May 2023
Source Universidade Lusófona de Humanidades e Tecnologias
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Heroin use has been related to brain dysfunction particularly in the prefrontal cortex. These effects are evident in neuropsychological impairments in attention, memory and executive functioning of heroin users. To assess these deficits and the application of a novel approach of cognitive stimulation to heroin users in treatment for opioid dependence, we have carried out a neuropsychological intervention program with mobile health technology. Patients diagnosed with opioid dependence were submitted to cognitive stimulation during four weeks in a three-day/week basis.

Recruitment information / eligibility
Status Completed
Enrollment 65
Est. completion date January 2020
Est. primary completion date January 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Only patients that scored higher than the cutoff values for their age on the Mini Mental Examination Test and with no clinical scores on the Symptoms Checklist Revised will be included in the study. Exclusion Criteria: - Patients with alcohol dependence or with history of previous neurological disorders will be excluded from the study. Patients will be also screened for minimal computer literacy.

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Mobile health cognitive stimulation

Locations
Country Name City State
Portugal Ares Do Pinhal-Associação De Recuperação De Toxicodependentes Sintra Lisboa

Sponsors (3)
Lead Sponsor Collaborator
Pedro Gamito Ares Do Pinhal-Associação De Recuperação De Toxicodependentes, Universidade Lusófona de Humanidades e Tecnologias

Country where clinical trial is conducted

Portugal, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in the results of Frontal Assessment Battery - FAB The participants were assessed in frontal lobe functions at the beginning of the rehabilitation and after 10 rehabilitation sessions, which had the approximate duration of one month. 1 month
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