Determination of the Minimal Detectable Change of the Parkinson's Disease Questionnaire-8

NCT ID: NCT06487364

Last Updated: 2025-03-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

39 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-05-13

Study Completion Date

2025-09-17

Brief Summary

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This study is conducted to determine how many units of improvement the Parkinson's Disease Questionnaire-8 (PDQ-8), used to evaluate the quality of life of Parkinson's patients, should have to express a significant change in the quality of life. Patients for whom a 30-session physiotherapy program is recommended will be included in the study. Patients will be asked to express the change in their quality of life at the end of treatment. The PDQ-8 survey and Global Rating of Patient-Perceived Changes (GRP-PC) forms will be used to determine these changes. Evaluations will be repeated at the beginning of the treatment program and at the end of the 30th session.

Detailed Description

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Conditions

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Parkinson Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Physiotherapy Group

There will be only one group in the study. Patients will only be applied to the physiotherapy program recommended by the specialist physician and physiotherapist. It is not possible to apply any additional treatment within the scope of the study.

Rehabilitation

Intervention Type OTHER

A routine physical therapy program prescribed by a specialist physician and physiotherapist will be applied.

Interventions

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Rehabilitation

A routine physical therapy program prescribed by a specialist physician and physiotherapist will be applied.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Having regular neurology follow-up and using medicine;
* Hoehn and Yahr Scale Stage between 1-3 points;
* Mini-Mental State Assessment Score \>24 points;

Exclusion Criteria

* Having a secondary neurological disease;
* Any surgery and/or trauma affecting the upper extremity
* Having complaints of pain before the treatment program;
* There was a change in medical treatment during the study;
* With symptoms of anxiety and depression;
* Those who use alcohol and drugs;
* Individuals with vision defects that cannot be corrected by the use of glasses and those with hearing loss
Minimum Eligible Age

40 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Emre Şenocak

OTHER

Sponsor Role lead

Responsible Party

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Emre Şenocak

Research Assisstant

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Murat Emirzeoğlu, PhD

Role: STUDY_CHAIR

Karadeniz Technical University

Adem Aktürk, PhD

Role: STUDY_CHAIR

İstanbul Gelişim University

Tuğba Eyigürbüz, PhD

Role: STUDY_CHAIR

Bağcılar Education and Research Hospital

Locations

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Private Güney Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Emre Şenocak, PhD

Role: CONTACT

+90 553 569 56 92

Facility Contacts

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Call Center, Personel of Call Center

Role: primary

+90 212 645 16 16

Adem Aktürk, PhD (Also: Medical Doctor)

Role: backup

+90 533 310 23 15

Other Identifiers

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2024/78

Identifier Type: -

Identifier Source: org_study_id

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