Skip to content

The Efficacy of Robot-Assisted Intelligent Rehabilitation Treatment in Patients With AUD

A Randomized Controlled Trial Protocol Testing the Efficacy of Robot-Assisted Intelligent Rehabilitation Treatment in Patients With Alcohol Use Disorders

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05675553
Enrollment
100
Registered
2023-01-09
Start date
2022-06-15
Completion date
2024-03-31
Last updated
2023-01-09

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

Conditions

Alcohol Use Disorder

Brief summary

We aimed to test the efficacy of robot-assisted intelligent rehabilitation treatment in patients with alcohol use disorders with a randomized controlled trial. Specifically, the objective of this trial is to determine whether the robot-assisted intelligent rehabilitation treatment plus treatment as usual has greater efficacy than traditional therapy in the treatment of alcohol use disorders.

Detailed description

Based on artificial intelligence technology, face recognition technology, and virtual reality technology to develop an available Robot-assisted rehabilitation intelligent system. Then, using this intelligent system as a new way of Psychotherapy to provide treatment for patients with alcohol use disorders, and compare with traditional treatment to verify the efficacy and safety of the Robot-assisted rehabilitation intelligent system in Chinese patients with alcohol use disorders.

Interventions

Participants assigned to this condition were offered 10 individual sessions of robot-assisted rehabilitation treatment, delivered by the Robot-assisted rehabilitation intelligent system. The system contains 10 core cognitive-behavioral therapy (CBT) skill topics (such as functional analysis, coping skills training, reviewing practice exercises, and explaining CBT concepts). A robot therapist demonstrates the target CBT skills and assigns homework to participants. The treatment framework is semi-structured through human-computer interaction. The forms of interaction include inquiries, statements, recommendations summaries, and knowledge assessments.

OTHERtreatment as usual

Both groups will receive treatment as usual, including medication, exercise, and psychological education.

Sponsors

Shanghai Mental Health Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

1. Between the ages of 18-55; 2. Meeting DSM-5 criteria for alcohol use disorders; 3. Withdrawing alcohol for less than 12 months; 4. Ability to use computers; 5. Signing informed consent;

Exclusion criteria

1. Having comorbidities of other neuropsychiatric diseases; 2. Diseases that affect cognitive function, such as a history of head trauma, cerebrovascular disease, epilepsy, etc. 3. With a family history of mental illness 4. Not familiar with computer operation, unable to complete assessment and treatment.

Design outcomes

Primary

MeasureTime frameDescription
Desire for alcohol3 monthsThe primary outcome is patients' desire for alcohol,measured by Visual Analogue Scale(VAS).

Secondary

MeasureTime frameDescription
Perception of stress3 monthsThe secondary outcome includes participants' perception of stress, measured by the Perceived Stress Scale(PSS).
Change Readiness and Treatment Eagerness3 monthsThe secondary outcome includes participants' Change Readiness and Treatment Eagerness, measured by the Stages of Change Readiness and Treatment Eagerness Scale(SOCRATES).
Impulsiveness3 monthsThe secondary outcome includes participants' level of impulsiveness, measured by the Barratt Impulsiveness Scale(Barratt).
Depression3 monthsThe secondary outcome includes the participants' level of depression, measured by Patient Health Questionnaire-9(PHQ-9).
Sleep Quality3 monthsThe secondary outcome includes participants' sleep quality, measured by Pittsburgh Sleep Quality Index(PSQI).
coping style3 monthsThe secondary outcome includes participants' coping style, measured by Simplified Coping Style Questionnaire(SCSQ).
use of alcohol3 monthsThe secondary outcome includes participants' use of alcohol.
Anxiety3 monthsThe secondary outcome includes the participants' level of anxiety, measured by generalized Anxiety Disorder-7(GAD-7).

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026