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CompletedNCT07887802Updated Oct 21, 2026

Multimodal Rehabilitation and Balance Assessment in Parkinson's Disease

An interventional study of Multimodal Rehabilitation Program in Parkinson Disease (PD), sponsored by Bilinç Doğruöz Karatekin. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-10-21.

Sponsored by Bilinç Doğruöz Karatekin · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 8 months after the study started (first participant enrolled Feb 2024, registered Oct 2026).
Updated Oct 21, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
18
Allocation
Not applicable
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This study aimed to investigate the relationship between instrumented balance measurements and clinical balance assessments in individuals with Parkinson's disease and to evaluate changes in balance and functional mobility following a 12-week multimodal rehabilitation program.

Eighteen individuals with Parkinson's disease participated in this prospective, single-group study. All participants received a rehabilitation program that included balance exercises, aerobic exercise, and balance training using the Korebalance system. The program was conducted twice weekly for 12 weeks.

Balance was assessed using the Korebalance system and the Berg Balance Scale (BBS). Functional mobility was evaluated using the Timed Up and Go (TUG) test. Assessments were performed before and after the rehabilitation program.

The study examined whether instrumented balance measurements were associated with clinical balance performance and whether balance and functional mobility changed following rehabilitation.

Read the detailed description

This prospective, single-center, single-group pre-post interventional study investigated instrumented balance assessment and changes in balance and functional mobility following multimodal rehabilitation in individuals with Parkinson's disease.

A total of 18 participants with Parkinson's disease were included. Eligible participants were adults aged 18 years or older with Hoehn and Yahr stages 1-3 who were able to participate in the rehabilitation program. Exclusion criteria included advanced Parkinson's disease (Hoehn and Yahr stages 4-5), significant cognitive impairment, other neurological disorders affecting balance, recent surgery within the preceding six months, and severe or uncontrolled systemic diseases that could interfere with participation.

All participants underwent a 12-week multimodal rehabilitation program consisting of two supervised sessions per week. The program included progressive static and dynamic balance exercises, functional mobility training, dual-task activities, moderate-intensity aerobic exercise, and balance training using the Korebalance system.

Balance training included tandem stance, single-leg stance when safely achievable, multidirectional weight shifting and stepping, repeated sit-to-stand exercises, obstacle negotiation, turning, and functional walking. More advanced activities included figure-of-eight walking, step negotiation, reactive postural control, and dual-task exercises combining motor and cognitive tasks. Aerobic training was performed using treadmill walking or stationary cycling at moderate intensity, generally corresponding to a Borg Rating of Perceived Exertion of 11-14.

The primary outcome measures were static and dynamic balance scores obtained using the Korebalance Premiere-19 system. Lower Korebalance scores indicated better balance performance.

Secondary outcome measures included the Berg Balance Scale (BBS), which assessed clinical balance, and the Timed Up and Go (TUG) test, which assessed functional mobility.

Outcome assessments were performed at baseline and after completion of the 12-week rehabilitation program.

Baseline instrumented balance measurements were examined in relation to clinical balance and functional mobility measures. Changes in instrumented balance, clinical balance, and functional mobility were evaluated by comparing measurements obtained before and after rehabilitation.

The study did not include randomization or a control group. All participants received the same multimodal rehabilitation intervention.

02

Conditions studied

  • Parkinson Disease (PD)

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Keywords

  • Parkinson's Disease
  • Balance Rehabilitation
  • Korebalance
  • Instrumented Balance Assessment
  • Berg Balance Scale
  • Timed Up and Go
  • Multimodal Rehabilitation
  • Postural Stability
03

In context

Parkinson Disease

4,583 studies on the registry are indexed under Parkinson Disease; 1,097 are open to participants now.

This study's enrollment of 18 is below the median of 40 across 3,365 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

This is the only study on the registry with Bilinç Doğruöz Karatekin as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults aged 18 years or older.
  • Diagnosis of Parkinson's disease.
  • Hoehn and Yahr stages 1-3.
  • Sufficient cognitive function to understand and follow instructions during assessments and rehabilitation.
  • Ability to participate in the rehabilitation program.
  • Provision of written informed consent.

Exclusion criteria

Exclusion Criteria:

  • Advanced Parkinson's disease (Hoehn and Yahr stages 4-5).
  • Significant cognitive impairment that could interfere with participation or assessment.
  • Other neurological disorders affecting balance or mobility.
  • History of surgery within the preceding six months.
  • Severe or uncontrolled systemic diseases that could interfere with safe participation in the rehabilitation program.
  • Refusal or inability to provide informed consent.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
18 participants (actual)

Study arms

  • Experimental
    Multimodal Rehabilitation Group

    Participants with Parkinson's disease received a 12-week supervised multimodal rehabilitation program, conducted twice weekly. The intervention included progressive balance exercises, functional mobility training, dual-task activities, moderate-intensity aerobic exercise, and Korebalance-assisted balance training. All participants received the same intervention, with no control group.

    Behavioral: Multimodal Rehabilitation Program

Interventions

  • BehavioralMultimodal Rehabilitation Program

    Participants received a supervised multimodal rehabilitation program twice weekly for 12 weeks (24 sessions). The program included approximately 10 minutes of warm-up exercises, 20 minutes of progressive balance training, and 20 minutes of moderate-intensity aerobic exercise using a treadmill or stationary bicycle. Balance exercises included static and dynamic balance tasks, multidirectional stepping, functional mobility activities, turning, and dual-task training. Additional balance training was performed using the Korebalance Premiere-19 system. Exercise intensity was generally maintained at a Borg Rating of Perceived Exertion of 11-14. Exercises were individually progressed according to participant ability and safety.

06

What researchers measure

Primary outcomes

  1. Change in Static Korebalance Score

    Static balance was assessed using the Korebalance Premiere-19 system. Measurements were obtained at baseline and after the 12-week multimodal rehabilitation program. Lower scores indicate better balance performance. Change was calculated as the post-intervention score minus the baseline score.

    Time frame: Baseline and Week 12

  2. Change in Dynamic Korebalance Score

    Dynamic balance was assessed using the Korebalance Premiere-19 system. Measurements were obtained at baseline and after the 12-week multimodal rehabilitation program. Lower scores indicate better balance performance. Change was calculated as the post-intervention score minus the baseline score.

    Time frame: Baseline and Week 12

Secondary outcomes

  1. Change in Berg Balance Scale Score

    Clinical balance was assessed using the Berg Balance Scale (BBS), which consists of 14 items evaluating static and dynamic balance during functional activities. Each item is scored from 0 to 4, resulting in a total score ranging from 0 to 56. Higher scores indicate better balance performance. Change was calculated as the post-intervention score minus the baseline score.

    Time frame: Baseline and Week 12

  2. Change in Timed Up and Go Test Time

    Functional mobility was assessed using the Timed Up and Go (TUG) test. Participants were instructed to stand up from a chair, walk 3 meters, turn around, return to the chair, and sit down. The time required to complete the test was recorded in seconds. Lower values indicate better functional mobility. Change was calculated as the post-intervention time minus the baseline time.

    Time frame: Baseline and Week 12

07

Study locations

1 site
  • Goztepe Prof. Dr. Suleyman Yalcin City Hospital
    Istanbul, 34722, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Feb 2024 to primary completion in Aug 2026, 30 months.

Of 1,296 non-industry interventional studies with no phase under Parkinson Disease, half reached primary completion within 24 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 45. This study's 30 months is above that.

Counting every sponsor, half of 1,369 studies reached it within 24 months; a quarter within 11 and three quarters within 44.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 15, 2026
First posted
Oct 21, 2026
StartActual
Feb 5, 2024
Primary completionActual
Aug 17, 2026
CompletionActual
Aug 17, 2026
Last update
Oct 21, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 21, 2026
Show all 1 update
  1. Oct 21, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07887802
Lead sponsor
Bilinç Doğruöz Karatekin
Responsible party
Bilinç Doğruöz Karatekin (Cihat Kurt, MD, Istanbul Medeniyet University) — Sponsor-investigator
First posted
Oct 21, 2026
Start date
Feb 5, 2024
Primary completion
Aug 17, 2026
Completion
Aug 17, 2026
Last update
Oct 21, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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