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Effect of Person-Centered Occupational Therapy Interventions for Substance Use Disorder

H

Hacettepe University

Status

Enrolling

Conditions

Substance Use Disorder (SUD)

Treatments

Behavioral: Awareness Training
Behavioral: Person-Centered Occupational Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT07364240
E-10840098-202.3.02-215

Details and patient eligibility

About

This study investigates the impact of person-centered occupational therapy interventions on individuals diagnosed with substance use disorder. Substance use often leads to isolation and difficulties in daily activities such as work, self-care, and leisure time. The research aims to evaluate how a tailored 8-week therapy program affects participants' occupational performance, self-efficacy, and psychological resilience. Participants will be divided into a study group receiving therapy and a control group.

Full description

Participants aged 18-65 with a DSM-5 diagnosis of substance use disorder will be recruited from the Erenköy AMATEM unit. The study employs an experimental design with 34 participants (17 in the study group, 17 in the control group). The study group will receive person-centered occupational therapy interventions 3 times per week for a total of 8 weeks.

The intervention process is based on the four stages of person-centered practice: identifying occupational performance problems using the Canadian Occupational Performance Measure (COPM), brainstorming realistic goals, implementing tailored strategies (e.g., time management, vocational skills, or healthy habits), and revising the process based on feedback . Assessment tools including the COPM, Self-Efficacy Scale, and Brief Resilience Scale will be administered at baseline and after the 8-week intervention to measure changes in performance and psychological factors.

Enrollment

34 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being diagnosed with substance use disorder according to DSM-5 criteria.
  • Having completed the detoxification process.
  • Being between the ages of 18-65.
  • Having at least a primary school education.
  • Volunteering to participate and signing the informed consent.

Exclusion criteria

  • Being in an acute psychotic episode.
  • Having severe neurological deficits that prevent responding to assessments. -Having severe visual or hearing loss that prevents completing the test batteries

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

34 participants in 2 patient groups

Study Group
Experimental group
Description:
Participants in this group will receive person-centered occupational therapy interventions in addition to their routine treatment.
Treatment:
Behavioral: Person-Centered Occupational Therapy
Control Group
Active Comparator group
Description:
Participants in this group will receive a one-time awareness training session about substance use disorder and its effects, in addition to their routine clinical follow-up.
Treatment:
Behavioral: Awareness Training

Trial contacts and locations

1

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Central trial contact

Onur Altuntaş, Assoc Prof; Büşra Yuvalı, PhD Cand

Data sourced from clinicaltrials.gov

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