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Not yet recruitingNCT07885774Updated Oct 23, 2026

UULEX Reliability in Individuals With Stroke

An observational study in Stroke, UULEX and Test-Retest Reliability, sponsored by Karabuk University. Not yet recruiting. Open to participants aged 18 Years to 78 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-23.

Sponsored by Karabuk University · Observational

Updated Oct 23, 2026Primary completion movedStudy completion moved+1 moreGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
30
Ages
18 Years to 78 Years
Sex
All
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Study summary

This study was designed to determine the test-retest reliability of the Unsupported Upper Limb Exercise Test (UULEX) in individuals with stroke. Motor impairments following stroke, particularly reductions in upper limb muscle strength, motor control, and functional performance, may adversely affect individuals' activities of daily living and functional independence. Therefore, the assessment of upper limb performance using reliable and feasible methods is important for planning and monitoring the rehabilitation process.

The UULEX is an incremental, performance-based, easy-to-administer, and low-cost field test developed to assess upper limb exercise capacity. Although the UULEX has been used in different clinical populations, evidence regarding its test-retest reliability in individuals with stroke is limited. In this study, the UULEX will be administered twice to individuals with stroke at a predetermined interval, and the consistency between the two measurements will be evaluated to determine its test-retest reliability. It is hypothesized that the UULEX will demonstrate high test-retest reliability in individuals with stroke. The findings of this study are expected to provide evidence regarding the reliability of the UULEX as a clinical assessment tool for evaluating upper limb exercise capacity in individuals with stroke.

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Conditions studied

  • Stroke
  • UULEX
  • Test-Retest Reliability

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03

In context

Stroke

7,441 studies on the registry are indexed under Stroke; 2,012 are open to participants now.

This study's planned enrollment of 30 is below the median of 160 across 1,729 observational studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

Karabuk University is the lead sponsor of 131 studies on the registry; 30 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 78 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population will consist of adults aged 18-78 years with stroke-related hemiplegia who meet the eligibility criteria and voluntarily agree to participate in the 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

  • Diagnosis of hemiplegia
  • Age between 18 and 78 years
  • Willingness to participate in the study

Exclusion criteria

Exclusion Criteria:

  • Presence of upper extremity or neck pain
  • Cognitive impairment
  • Presence of comorbidities affecting upper extremity and hand function (carpal tunnel syndrome, trigger finger, impingement syndrome, thoracic outlet syndrome, lateral or medial epicondylitis)
  • History of upper extremity surgery
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Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
30 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • Hemiplegia group

    Individuals diagnosed with hemiplegia, aged 18-78 years, and willing to participate were included in the study, whereas those with upper extremity or neck pain, cognitive impairment, comorbidities affecting upper extremity and hand function (carpal tunnel syndrome, trigger finger, impingement syndrome, thoracic outlet syndrome, or lateral or medial epicondylitis), or a history of upper extremity surgery were excluded.

    Diagnostic Test: Unsupported Upper Limb Exercise Test [UULEX]

Interventions

  • Diagnostic testUnsupported Upper Limb Exercise Test [UULEX]

    The UULEX consists of eight horizontal levels positioned 15 cm apart. Participants are seated facing the chart and raise a 0.2-kg bar from hip level to progressively higher levels at a rate of 30 movements per minute using a metronome. After a 2-min warm-up, the level is increased every minute. Once the highest level is reached, the load is increased by 0.5 kg each minute up to 2 kg. The test continues until symptom limitation or a maximum of 12 min. For reliability assessment, the UULEX will be performed three times using the same standardized protocol. The first two assessments will be conducted on the same day with a 1-h rest interval, and the third will be performed one week later.

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What researchers measure

Primary outcomes

  1. Test-Retest Reliability of the Unsupported Upper Limb Exercise Test (UULEX)

    Upper limb exercise capacity will be assessed using the Unsupported Upper Limb Exercise Test (UULEX). Participants will perform progressive unsupported upper limb exercise until symptom limitation or the maximum test duration is reached. UULEX performance will be recorded as total test duration (seconds). The test will be performed three times: twice on the same day with a 1-hour interval and once one week later. Test-retest reliability will be determined by comparing UULEX performance across assessments.

    Time frame: The UULEX will be administered three times to each participant: the first and second assessments will be performed with a 1-hour rest interval, and the third assessment will be conducted one week later.

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Study locations

No study locations are listed for this record.

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References and documents

Publications

  • Karazeybek ZB, Naz I. Convergent Validity and Test-Retest Reliability of the Unsupported Upper Limb Exercise Test in Patients with Chronic Neck Pain. Percept Mot Skills. 2022 Aug;129(4):1177-1192. doi: 10.1177/00315125221096400. Epub 2022 Apr 27. PubMed 35473433 ↗
  • Cetin SY, Basakci Calik B, Ayan A, Cavlak U. Validity and reliability of the unsupported upper-limb exercise test in individuals with rheumatoid arthritis. Int J Rheum Dis. 2019 Nov;22(11):2025-2030. doi: 10.1111/1756-185X.13720. Epub 2019 Oct 9. PubMed 31595690 ↗
  • Fulton I, McEvoy M, Pieterse J, Williams M, Thoirs K, Petkov J. Transversus abdominis: changes in thickness during the unsupported upper limb exercise test in older adults. Physiother Theory Pract. 2009 Nov;25(8):523-32. doi: 10.3109/09593980802665023. PubMed 19925260 ↗
  • Lima VP, Velloso M, Almeida FD, Carmona B, Ribeiro-Samora GA, Janaudis-Ferreira T. Test-retest reliability of the unsupported upper-limb exercise test (UULEX) and 6-min peg board ring test (6PBRT) in healthy adult individuals. Physiother Theory Pract. 2018 Oct;34(10):806-812. doi: 10.1080/09593985.2018.1425786. Epub 2018 Jan 19. PubMed 29351493 ↗
  • Takahashi T, Jenkins SC, Strauss GR, Watson CP, Lake FR. A new unsupported upper limb exercise test for patients with chronic obstructive pulmonary disease. J Cardiopulm Rehabil. 2003 Nov-Dec;23(6):430-7. doi: 10.1097/00008483-200311000-00007. PubMed 14646791 ↗

Individual participant data

Plan to share: No — De-identified individual participant data may be made available from the corresponding author upon reasonable request.

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Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedDate before it movedWhere the date was before it movedSimilar 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

Start is estimated for Oct 2026; primary completion for Nov 2026, 0 months later.

Of 787 non-industry observational studies under Stroke, half reached primary completion within 43 months of starting (the median), counting those still running; a quarter within 18 and three quarters within 101. This study's planned 0 months is below that.

Counting every sponsor, half of 833 studies reached it within 41 months; a quarter within 18 and three quarters within 92.

Since we started tracking on Sep 25, 2026, the dates moved once, on Oct 23, 2026: primary completion Dec 2026 → Nov 2026 and completion Dec 2026 → Nov 2026.

Earlier changes are on the record history on ClinicalTrials.gov ↗

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

Registered
Oct 13, 2026
First posted
Oct 21, 2026
StartEst.
Oct 26, 2026
Primary completionEst.
Nov 20, 2026was Dec 2026
CompletionEst.
Nov 26, 2026was Dec 2026
Last update
Oct 23, 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.
Primary completion
Dec 1, 2026→Nov 20, 2026
Oct 23, 2026
Study completion
Dec 26, 2026→Nov 26, 2026
Oct 23, 2026
Registered
First appeared on the registry
Oct 21, 2026
Show all 2 updates
  1. Oct 23, 2026
    Primary completion Dec 1, 2026→Nov 20, 2026
    Study completion Dec 26, 2026→Nov 26, 2026
    + 2 other changes: verification date and references
  2. 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 ↗

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Registry details

Key details

Study ID
NCT07885774
Lead sponsor
Karabuk University
Responsible party
Nurcan Contarli (Assistant Professor, Karabuk University) — Principal investigator
First posted
Oct 21, 2026
Start date
Oct 26, 2026 (estimated)
Primary completion
Nov 20, 2026 (estimated)
Completion
Nov 26, 2026 (estimated)
Last update
Oct 23, 2026

Study contacts

Nurcan Contarli, Assistant Professor
Contact
nurcancontarli@karabuk.edu.tr
03704189171

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 not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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