The effect of occupational therapy interventions on participation in people with idiopathic Parkinson's disease

Comparison of the effects of occupation-based interventions with and without responsibility feedback and conventional interventions on participation in people with idiopathic Parkinson’s disease

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20140304016830N13

Enrollment

Registered

2022-08-19

Start date

2022-08-29

Completion date

Unknown

Last updated

2022-08-29

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

Conditions

Parkinson's disease. Parkinson's disease

Interventions

Intervention 1: First Intervention group: This group will receive occupation-based interventions with responsibility feedbacks for 24 sessions (12 weeks, two sessions per week). Participants will rece

Eligibility

Sex/Gender

All

Age

35 Years to 85 Years

Inclusion criteria

Inclusion criteria: Diagnosis of idiopathic Parkinson’s disease based on UK Brain Bank criteria according to neurologist Disease progression level based on Hoehn and Yahr stages of I to III Acceptable cognitive function (a score of > 24 on Montreal Cognitive Assessment Ability to read and write in Persian to complete self-reported questionnaires

Exclusion criteria

Exclusion criteria: Atypical parkinsonian syndromes Other existing neurological disorders, such as stroke Juvenile Parkinson’s Disease Impulsive-compulsive disorders

Design outcomes

Primary

Measure	Time frame
Participation satisfaction. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Utrecht Scale for Evaluation of Rehabilitation-Participation Satisfaction.	—

Secondary

Measure	Time frame
Participation frequency and restriction. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Utrecht Scale for Evaluation of Rehabilitation-Frequency and restriction scales.;Self-perceived performance and performance satisfaction. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Canadian Occupational Performance Measure.;Motivation. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Social Motivation Questionnaire.;Volition. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Volitional Questionnaire.;Sense of agency. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Intentional Binding Task.;Responsibility. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Allocation of Treatment Responsibility Scale.;Physical activity. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Phone Frequency, Intensity, Time, and Type (Phone-FITT) Questionnaire.;Community integration. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Community Integration Questionnaire-Revised.;Activities of daily living and Instrumental activities of daily living. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Nottingham Extended ADL Scale.;Upper extremity function. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: 9-hole peg Test.;Fatigue. Timepoint: Baseline, session 9, session 17, post-intervention (week 1	—

Measure

Time frame

Participation frequency and restriction. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Utrecht Scale for Evaluation of Rehabilitation-Frequency and restriction scales.;Self-perceived performance and performance satisfaction. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Canadian Occupational Performance Measure.;Motivation. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Social Motivation Questionnaire.;Volition. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Volitional Questionnaire.;Sense of agency. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Intentional Binding Task.;Responsibility. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Allocation of Treatment Responsibility Scale.;Physical activity. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Phone Frequency, Intensity, Time, and Type (Phone-FITT) Questionnaire.;Community integration. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Community Integration Questionnaire-Revised.;Activities of daily living and Instrumental activities of daily living. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: Nottingham Extended ADL Scale.;Upper extremity function. Timepoint: Baseline, session 9, session 17, post-intervention (week 13), and follow-up (week 25). Method of measurement: 9-hole peg Test.;Fatigue. Timepoint: Baseline, session 9, session 17, post-intervention (week 1

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactGhorban Taghizadeh

Iran University of Medical Sciences

taghizadeh.gh@iums.ac.ir+98 21 2222 7124

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 8, 2026