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Parkinson DiseaseNCT06562686

Assessment of Methods Used in Evaluating Balance Rehabilitation in Parkinson's Patients

An observational study of Parkinson Disease, run by Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Balance rehabilitation holds an important place in the treatment of Parkinson's patients. Before and after treatment, patients are evaluated using various measurement methods. In calculations of changes post-treatment, although statistically significant changes are detected, clinical differences are often not… Read more about this study

Who is it for?
Ages 50 to 80 years
Conditions the study is for
Parkinson Disease
How many people
83 participants
Where
1 siteTurkey (Türkiye)
Study dates
Aug 2024to Jul 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 50 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Your study plans to include patients who meet the inclusion criteria and voluntarily participate in the research. These patients will be recruited from the Parkinson's Disease specialized outpatient clinic of the Department of Physical Medicine and Rehabilitation at Sultan Abdulhamid Han Training and Research Hospital, Health Sciences University, starting from August 1, 2024. They will have been prescribed conventional therapy for balance improvement, robot-assisted walking therapy, or a home exercise program by a specialist physician.

Who may be able to join

  • Diagnosis of Parkinson's disease
  • Aged between 50-80 years
  • Modified Hoehn and Yahr stage 1.5 - 3
  • On stable medical treatment for the last 3 months
  • Mini-Mental State Examination score > 23
  • Approval of the informed consent form

Who cannot join

  • Age below 50 or above 80 years
  • Musculoskeletal disorders, severe osteoarthritis, peripheral neuropathy, or history of -previous lower extremity joint replacement
  • Cardiovascular disease, especially uncontrolled hypertension exceeding 180/110 mm Hg at rest within the last four weeks, or recent myocardial infarction
  • Orthostatic hypotension
  • Body weight exceeding 100 kg
  • Respiratory system disease
  • Presence of severe dyskinesia, visual impairment, and uncontrolled on-off fluctuations

Trial locations and contacts

1 site in 1 country.

Zeynep Candan, M.D. contact

05395955090

drzeynepcandan@gmail.com

Turkey (Türkiye)1 site
  • Zeynep Candan

    Istanbul

    zeynep candan, 05395955090, drzeynepcandan@gmail.com

Other trials in Turkey (Türkiye)

About this study

Official title: Assessment of Methods Used in Evaluating Balance Rehabilitation in Parkinson's Patients: Determination of Responsiveness and Minimal Clinically Important Difference Values

Balance rehabilitation holds an important place in the treatment of Parkinson's patients. Before and after treatment, patients are evaluated using various measurement methods. In calculations of changes post-treatment, although statistically significant changes are detected, clinical differences are often not observed. Jaeschke et al. developed the concept of minimal clinically important difference (MCID) to address this. They have worked on methods to determine the level of MCID. These measurements help clinicians understand which results can be interpreted as clinically meaningful for the patient.

Responsiveness refers to how sensitive a measurement tool is to changes, whereas MCID focuses on determining whether these changes are clinically significant. Both concepts are crucial for understanding and interpreting the performance of measurement tools.

Identifying which patients have a high risk of balance problems and falls, and screening those at risk, is important for making treatment decisions. Determining which change values are clinically significant (MCID) and identifying which tests are more sensitive in detecting changes (responsiveness) are essential in monitoring patients.

Read the detailed description

Parkinson's disease (PD) is a chronic progressive neurodegenerative disease characterized by the degeneration or loss of dopaminergic neurons in the nigrostriatal and other neuronal systems, along with the formation of Lewy bodies in dopaminergic neurons, and it manifests with both motor and non-motor symptoms and findings. It is the second most common neurodegenerative disease after Alzheimer's disease. The average onset age is between 60-80 years. It is more commonly seen in men and the white race. In Turkey, the prevalence has been reported as 111/100,000. In societies where the average lifespan is increasing, the frequency of PD and the associated economic burden are also expected to increase.

The etiology of Parkinson's disease includes environmental, genetic, and aging-related processes. These factors trigger mechanisms leading to neuron degeneration and loss, causing PD.

The clinical presentation of Parkinson's disease consists of motor and non-motor symptoms and findings. The main motor symptoms are bradykinesia, rigidity, postural instability, and resting tremor. Other observed findings include akinesia, freezing phenomenon, postural and gait disorders, reciprocal movement disorder, masked facial expression, impaired orofacial functions and speech, swallowing disorder, respiratory function impairment, loss of hand dexterity, and coordination. Cognitive impairments, depression, sleep disorders, autonomic dysfunction, loss of smell, fatigue, and sialorrhea are among the non-motor symptoms.

Patients with primary motor findings and accompanying symptoms are evaluated using the Parkinson's Disease United Kingdom Brain Bank Criteria and the National Institute of Neurological Disorders and Stroke (NINDS) diagnostic criteria. A definitive diagnosis is made by pathologically demonstrating Lewy bodies in a biopsy. The Hoehn-Yahr Scale is frequently used to determine the severity of the disease.

The treatment of Parkinson's disease includes medical treatment, surgical treatment, and rehabilitation. Rehabilitation plays an important role at all stages of PD. In the early stages, it helps maintain well-being and improve general conditioning; in the later stages, it is crucial for coping with motor and non-motor complications.

Postural instability and balance disorders in Parkinson's patients lead to sudden falls, progressive disability, and immobility. Patients' fear of falling causes them to limit their activities, which increases immobility and balance problems. Preventing falls and maintaining mobility should involve a multidisciplinary treatment and rehabilitation program. Various rehabilitation approaches are available, including conventional therapy, music therapy, aquatic therapy, dance therapy, virtual reality therapy, robot-assisted gait therapy, and tai chi. Many studies in the literature evaluate the effectiveness of rehabilitation approaches aimed at balance and mobility in Parkinson's disease.

Balance disorders are a significant motor problem in individuals with PD. It is necessary to identify at-risk patients through appropriate tests and to organize treatment accordingly. Although there are many scales available to evaluate patients' balance to determine their rehabilitation needs, there is no clarity on which scale(s) are more sensitive in assessing changes. Additionally, knowing which change scores in the scales the investigators use are clinically significant is important for evaluating treatment outcomes. Knowing the sensitivity and minimal clinically important difference (MCID) values of tests for balance and fall concerns in Parkinson's patients can guide clinicians in selecting scales for screening patients before treatment and understanding which changes are clinically significant when evaluating outcomes after treatment.

In 1989, Jaeschke et al. developed the concept of minimal clinically important difference (MCID). Jaeschke and colleagues noted that, while statistically significant changes were often detected in post-treatment change calculations, clinically significant differences were not observed and attempted to determine the smallest clinically important change level. This allowed patients to directly participate in the process of evaluating their condition. These measurements help clinicians understand which treatments yield better results. MCID is the smallest change that a patient would identify as important and that would indicate a difference in the patient's management. After R. A. Fisher defined the p-value and the 0.05 cutoff point, all clinical studies began to evaluate whether results were statistically significant, but the p-value, despite being an objective result, has two major issues. One is failing to detect a difference due to insufficient sample size despite an important difference (Type II error), and the other is that the statistically significant difference does not actually represent a meaningful change for the patient. Therefore, statistical significance may not carry clinical importance. MCID helps clinicians determine whether a treatment has a meaningful effect on the patient. Additionally, MCID is a valuable tool in planning scientific studies and calculating sample size. Understanding the minimal clinically important difference helps researchers design studies that are both significant and applicable to clinical practice. In summary, MCID is a critical concept that bridges clinical practice and research, emphasizing the impact of treatments from the patient's perspective. Understanding and applying MCID is essential for making correct treatment decisions and conducting meaningful scientific studies in healthcare. It is important to remember that the concept of MCID is variable and can differ between health conditions. In recent years, clinicians and researchers have started to focus on patient-reported outcome assessments.

The investigators also aim to determine the MCID values of measurement tools used to evaluate balance in Parkinson's disease in our study.

There are two commonly used methods for calculating MCID:

Anchor-based approach Distribution-based approach In the anchor-based approach, a comparison is made between a result measure reflecting the patient's condition (e.g., post-treatment measurement value) and an external criterion. This external criterion can be the patient's own perception or the clinician's assessment. In this method, changes between scores are compared with an anchor question that serves as a reference to determine whether the patient has improved compared to baseline. To understand the perception of change, a global rating scale ("much worse," "a little worse," "almost the same," "a little better," and "much better") can be used. The anchor question should be easily understandable and relevant to patients.

The distribution-based approach attempts to estimate the likelihood that a detected difference in measurement tools is meaningful. It uses statistical data such as fractions of standard deviation, effect size, and mean standard error. It does not include the perceptions based on the experiences of experts or patients. Since it does not include individual patient perceptions, it should not be the first choice for determining MCID. In this method, as there is no anchor question to evaluate what is important for patients, significant and clinically meaningful results cannot be defined. In fact, scores calculated with distribution-based methods are sometimes referred to as "minimal detectable change" instead of MCID. Therefore, this method is not recommended as the first choice for determining MCID.

However, some authors have suggested that a single MCID value can be misleading and that providing a range might be more appropriate. For this reason, in our study, the investigators will use both anchor-based and distribution-based approaches to calculate MCID, aiming to find a range of values. In the anchor-based approach, the investigators plan to use two anchor questions: a patient-based and a clinician-based global assessment scale.

Responsiveness refers to the ability of a measurement tool to detect true changes among individuals. A sensitive scale responds accurately to the changes experienced. Responsiveness is typically assessed using statistical analyses such as effect size and standard deviation and is used to evaluate the performance of measurement tools.

While responsiveness indicates how sensitive a measurement tool is to changes, MCID indicates whether these changes are meaningful from the patient's or clinician's perspective. In other words, a responsive measurement tool has the potential to capture clinically significant changes. Both concepts are important for understanding and interpreting the performance of measurement tools. Determining the responsiveness and MCID of a measurement tool provides clinicians with a more comprehensive assessment in research studies and patient follow-up.

Keywords
balance, Biodex balance system, Responsiveness, MCID, Parkinson's disease
Medical subject headings
Parkinson Disease

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Biodex

    Determination of the minimal clinical important change values of balance scores (fall risk test) determined by the Biodex balance system in Parkinson's disease

    Measured: One Month

Secondary outcomes (2)
  1. International Fall Activity Scale

    Determination of the minimal clinical important change values of tests assessing falls

    Measured: One Month

  2. timed up and go test

    Determination of the minimal clinical important change values of functional balance assessment tests

    Measured: One Month

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Aug 2024
  2. Study startAug 2024 (estimated)
  3. Primary completionApr 2025 (estimated)
  4. Study completionJul 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
83 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06562686
Sponsor's protocol ID
2024/7/7/19
Status last verified
Aug 2024
First submitted
12 Jul 2024
Last updated
20 Aug 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Jaeschke R, Singer J, Guyatt GH. Measurement of health status. Ascertaining the minimal clinically important difference. Control Clin Trials. 1989 Dec;10(4):407-15. doi: 10.1016/0197-2456(89)90005-6.

    PubMed 2691207
  • Godi M, Arcolin I, Giardini M, Corna S, Schieppati M. Responsiveness and minimal clinically important difference of the Mini-BESTest in patients with Parkinson's disease. Gait Posture. 2020 Jul;80:14-19. doi: 10.1016/j.gaitpost.2020.05.004. Epub 2020 May 17.

    PubMed 32464537
  • Donoghue D; Physiotherapy Research and Older People (PROP) group; Stokes EK. How much change is true change? The minimum detectable change of the Berg Balance Scale in elderly people. J Rehabil Med. 2009 Apr;41(5):343-6. doi: 10.2340/16501977-0337.

    PubMed 19363567

Questions about this trial

What is this clinical trial studying?

An observational study of Parkinson Disease, run by Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 20 Aug 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Zeynep Candan, M.D. (05395955090, drzeynepcandan@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Biodex (time frame: One Month). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06562686, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Aug 2024.

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Clinical Trial NCT06562686 | AzTrials