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TerminatedNCT06756958Updated Jan 3, 2025

Reliability and Validity of Pittsburgh Rehabilitation Participation Scale During Robot Therapy

An observational study in Stroke, sponsored by National Rehabilitation Center, Seoul, Korea. Terminated at 2 sites in Korea, Republic of. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-01-03.

Sponsored by National Rehabilitation Center, Seoul, Korea · Observational

Why this study was terminated
The researcher, who recruit, resigned.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
46
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 20 studies in Stroke by National Rehabilitation Center, Seoul, Korea — none open to participants now, none under way, none of them phase 3. Stroke · National Rehabilitation Center, Seoul, Korea.

Started
2017
with 2 others
Observational
Only one
of the 20
Registered
20th of 20
by date

Among the 20 studies in Stroke by National Rehabilitation Center, Seoul, Korea, this one is one of 3 that started in 2017, is the only observational one, and was the 20th registered.

Stroke

8,255 studies on the registry are indexed under Stroke; 2,056 are open to participants now.

Browse Stroke studies →

Open to participants now

None of the 20 studies in Stroke by National Rehabilitation Center, Seoul, Korea is open now. The open studies under Stroke, anywhere →

Where they have run

Who these studies take

Of the 1,415 Stroke studies recruiting now, 697 (49%) set no upper age limit and 280 (20%) stop at 75 or younger; 77 take children under 18; 196 take healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

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Download CSVNarrow it in search →With an account: the 20 studies in Stroke by National Rehabilitation Center, Seoul, Korea as a file.
02

Study summary

Reliability and validity of Pittsburgh Rehabilitation Participation Scale during robot therapy among patients with stroke

03

Conditions studied

  • Stroke

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Keywords

  • participation
  • robot
  • scale
  • rehabilitation
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Those who participated the tethered-robot assisted gait training, had the history of brain lesion and adimitted in the rehabilitation center.

Those who gave the informed consent about this study.

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

  • patients with stroke or traumatic brain injury
  • inpatient in rehabilitation center

Exclusion criteria

Exclusion Criteria:

  • brain tumor
  • spinal cord injury
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
46 participants (actual)
Patient registry
No

Interventions

  • OtherNo intervention (observational study)

    No intervention (observational study: The study participants were inpatient and were given robot-assisted gait training routinely.)

06

What researchers measure

Primary outcomes

  1. Pittsburgh Rehabilitation Participation Scale

    Pittsburgh Rehabilitation Participation Scale could be 1 (none), 2, 3, 4, 5, or 6 (excellent). Excellent (6): If the patient participated in all exercises or activities with maximal effort, finished all exercises or activities, and actively took interest in exercises or activities and/or future therapy sessions. None (1): patient refused entire session, or did not participate in any exercises or activities in session. In this study, a participant typically gets 12 sessions of robot assisted gait training. Just after the each session, Pittsburgh Rehabilitation Participation Scale is assigned as 1 to 6. For example, in a virtual case, the participant gets the score of 1, 1, 2, 2, 3, 3, 4, 4, 5, 5, 6, and 6 (median =3.5). the participant gets 12 numbers of outcome score and median of Pittsburgh Rehabilitation Participation Scale.

    Time frame: through study completion, an average of 3 year

Secondary outcomes

  1. modified Barthel Index

    Modified Barthel Index measures basic activities of daily life. Lowest score is zero and means no function. Highiest score is 100, best function.

    Time frame: baseline and 4 weeks from baseline

  2. 10m walk

    Time frame: baseline and 4 weeks from baseline

  3. Borg scale

    Borg scale measures perceived exertion during the test. It ranges 13 to 20. 13 means easy. 20 means hardest.

    Time frame: baseline and 4 weeks from baseline

  4. 6 min walk

    Time frame: baseline and 4 weeks from baseline

  5. motricity index

    Time frame: baseline and 4 weeks from baseline

  6. Berg balance scale

    Berg balance scale is the combination of 16 5-point-Likert-scale-like ordinal scale of 0 to 4. O means no balance. 56 means the maximal balance as the criteria.

    Time frame: baseline and 4 weeks from baseline

  7. Trunk impairment scale

    Scores range from a minimum of 0 to a maximum of 23. Zero means no balance. 23 means maximal balance and trunk function.

    Time frame: baseline and 4 weeks from baseline

  8. Function in sitting test

    Time frame: baseline and 4 weeks from baseline

  9. Modified Rankin Scale for Neurologic Disability

    Modified Rankin Scale for Neurologic Disability could be 0, 1, 2, 3, 4, 5, or 6. Zero (0) means no negative symptoms et al as the criteria. 6 means means dead condition (death) as the criteria.

    Time frame: baseline and 4 weeks from baseline

  10. Functional Ambulatory Category

    Time frame: baseline and 4 weeks from baseline

  11. Timed Timed Up and Go test

    Time frame: baseline and 4 weeks from baseline

  12. Manual Muscle Testing

    Time frame: baseline and 4 weeks from baseline

  13. modified Ashworth scale

    Modified Ashworth scale could be 0, 1, 1+, 2, 3, or 4. Zero (0) means no spasticity as the criteria. 4 means means maximal spasticity as the criteria.

    Time frame: baseline and 4 weeks from baseline

  14. National Institutes of Health Stroke Scale

    0 to 24 points. Zero (0) means no deficits as the criteria. 24 means means maximal deficits as the criteria.

    Time frame: baseline and 4 weeks from baseline

07

Study locations

2 sites
  • National Rehabilitation Center
    Seoul, 01022, Korea, Republic of
  • Jung Hwan Kim
    Seoul, 142884, Korea, Republic of
08

References and documents

Individual participant data

Plan to share: No

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Sep 2017 to primary completion in Oct 2021, 49 months.

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

Registered
Nov 10, 2024
First posted
Jan 3, 2025
StartActual
Sep 1, 2017
Primary completionActual
Oct 31, 2021
CompletionActual
Oct 31, 2021
Last update
Jan 3, 2025
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.
No changes since tracking began. The registry record was last updated on Jan 3, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06756958
Lead sponsor
National Rehabilitation Center, Seoul, Korea
Responsible party
Kim, Jung Hwan (Team manager, National Rehabilitation Center, Seoul, Korea) — Principal investigator
First posted
Jan 3, 2025
Start date
Sep 1, 2017
Primary completion
Oct 31, 2021
Completion
Oct 31, 2021
Last update
Jan 3, 2025

Oversight

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

Not currently enrolling

This study is terminated, as verified in Dec 2024. You cannot join it, but the record below documents what was studied.

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