None listed
Conditions
Interventions
Behavioral : This study's intervention involves the use of a smartphone application based on cognitive-behavioral therapy (CBT), aiming to evaluate its effects on alcohol abstinence maintenance and re
Sponsors
Hallym University Medical Center- Chuncheon
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Selection Criteria for Participants a) Adults aged 19 or older b) Individuals who meet the diagnostic criteria for Alcohol Use Disorder in DSM-5 and have been diagnosed with mental and behavioral disorders due to alcohol use (F10) according to ICD-10 c) Individuals who have no difficulty reading and writing in Korean d) Individuals who are able to use mobile applications on universal devices (such as smartphones or tablets) without difficulty e) Individuals who, after receiving sufficient explanation and understanding of the clinical trial, voluntarily decide to participate and agree in writing to comply with the precautions f) Individuals who are not diagnosed with dementia according to the judgment of a clinical doctor g) Individuals who, after receiving a detailed explanation about the study and fully understanding it, voluntarily decide to participate in the research and provide written consent, or their legal representatives do so Note: Additional selection criteria may be included depending on the features and target population of the developed smartphone application therapeutic device.
Exclusion criteria
Exclusion criteria: a) Any advanced, severe, progressive, or unstable disease that could put the patient at risk b) Any medical or other neurological conditions that could explain cognitive decline (e.g., abnormal thyroid function tests, vitamin B12 or folate deficiency, post-traumatic conditions, Huntington's disease, multiple sclerosis, cerebral palsy, encephalitis, meningitis, or any diseases affecting the central nervous system) c) Any other primary neurodegenerative dementias, excluding depression, schizophrenia, or bipolar disorder, including all other DSM-V Axis I diagnoses d) Individuals currently having uncontrolled seizure disorders e) Individuals with a history of brain injury resulting in a loss of consciousness for more than 1 hour or hospitalization within the past 3 years f) Hearing or vision impairments that may interfere with the performance of the required tasks in the clinical trial g) Individuals deemed unsuitable for the study according to the judgment of the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Maintenance of Abstinence for 9 to 12 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| AUDIT-K Scores;AUQ-K Scores;CIWA-Ar Scores;HADS Scores;CRQ Scores;HAIS Scores;K-BADS Scores;SOCRATES-K Scores;K-MAAS Scores | — |
Countries
Korea, Republic of
Contacts
Public ContactSong-Hee Lim
Hallym University Medical Center- Chuncheon
Outcome results
None listed