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Renal Transplanted RecipientsNCT06707792

Validity and Reliability of 6 Minute Stepper Test in Kidney Transplant Recipients

An observational study of Renal Transplanted Recipients, run by Hacettepe University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of our study was to investigate the validity and reliability of the 6 minute stepper test in kidney transplant recipients. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Renal Transplanted Recipients
How many people
45 participants
Where
1 siteTurkey (Türkiye)
Study dates
9 Jun 2024to 14 Dec 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 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Kidney transplant recipients will be included.

Who may be able to join

  • Patients with kidney transplantation
  • At least 6 months after the kidney transplant
  • Voluntary participation in the study

Who cannot join

  • Having a musculoskeletal problem that may interfere with the tests
  • Having neurological impairment
  • Having chronic lung disease
  • Having had any cardiovascular event in the last 6 months

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Hacettepe University

    Ankara

Other trials in Turkey (Türkiye)

About this study

Official title: Investigation of Validity and Reliability of 6 Minute Stepper Test in Kidney Transplant Recipients

The aim of our study was to investigate the validity and reliability of the 6 minute stepper test in kidney transplant recipients.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT06707792
Study groupRoleWhat they receive
Kidney transplant recipientsNot described

What is being measured

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

  1. Exercise capacity

    Exercise capacity will be assessed with a 6 minute stepper test.

    Measured: Day 1

  2. Exercise capacity

    Exercise capacity will be assessed with a 6 minute walk test.

    Measured: Day 1

  3. Peripheral muscle strength

    Knee extensor strength will be measured using a portable portable handheld dynamometer.

    Measured: Day 1

  4. Lower extremity endurance

    It will be evaluated with a one-minute sit to stand test.

    Measured: Day 1

Timeline

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

  1. First posted27 Nov 2024
  2. Study start9 Jun 2024
  3. Primary completion8 Nov 2025
  4. Study completion14 Dec 2025

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
Case only
Time perspective
Cross-sectional
Enrolment
45 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06707792
Sponsor's protocol ID
GO 23/604
Status last verified
Nov 2024
First submitted
25 Nov 2024
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Renal Transplanted Recipients, run by Hacettepe University 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 3 inclusion and 4 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: finished, as of the sponsor's last update on 20 Oct 2026. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Exercise capacity (time frame: Day 1). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 Oct 2026.

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