Running Related InjuriesNCT04743713
Turkish Cross-cultural Adaptation, Validation and the Reliability of UWRI (University of Wisconsin Running Injury and Recovery Index)
An observational study of Running Related Injuries, run by Hacettepe University at 1 site in Turkey (Türkiye).
Trial summary
The purpose is to perform a scientific study on TURKISH cross-cultural adaptation, validation and the reliability of UWRI Read more about this study
- Who is it for?
- Ages 14 to 45 years
- Conditions the study is for
- Running Related Injuries
- What is being tested?
- UWRI-Tr
- How many people
- 90 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 10 Feb 2021to 16 Jan 2022
- How long will I take part?
- 7 Days
- 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 14 to 45 years
- All sexes
- No healthy volunteers
- Child, Adult
Study population: Runners
Who may be able to join
- 14-45 years old female or male
- Participating in running as amateur, recreational, competitional or professional runner
- Being a short, mid, or long distance runner
- Being native Turkish speaker
- Agreed to participate in the research
Who cannot join
- If there is no surgical history related to running injury in the last 12 months
- If have chronic metabolic disease
- Paralympic athletes
- Pregnant and breastfeeding
Trial locations and contacts
1 site in 1 country.
About this study
The purpose is to perform a scientific study on TURKISH cross-cultural adaptation, validation and the reliability of UWRI
Read the detailed description
The primary aim of this study is to perform Turkish cross-cultural adaptation, validation and the reliability of UWRI in runners. The secondary aim of this study is investigating injury rate and types among runners.
- Conditions
- Running Related Injuries
- Being tested
- UWRI-Tr
- Keywords
- validity, reliability, PRO, Patient Outcome Report, Turkish, Adaptation, Running, Injury
- Medical subject headings
- Wounds and Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
UWRI-TrOther
Questionnaire
What is being measured
The primary outcome is the main question the study is designed to answer.
Validity and reliability
pearson's correlation 2 tailed analysis; >0,60 good, 0,31-0,59 medium, <0,30 bad
Measured: 5-7 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Feb 2021
- Study start10 Feb 2021 (estimated)
- Primary completion16 Jan 2022 (estimated)
- Study completion16 Jan 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Running Related InjuriesStudies of the same condition, open and under way.
- More trials run by Hacettepe UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Other
- Time perspective
- Prospective
- Enrolment
- 90 participants (estimated)
- Target duration
- 7 Days
Sponsor and investigators
- Lead sponsor
- Hacettepe University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Elif Turgut, Hacettepe University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04743713
- Sponsor's protocol ID
- GO 21/27
- Status last verified
- Feb 2021
- First submitted
- 3 Feb 2021
- Last updated
- 8 Feb 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 Feb 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Turkish Cross-cultural Adaptation, Validation and the Reliability of UWRI (University of Wisconsin Running Injury and Recovery Index)
- ClinicalTrials.gov ID
- NCT04743713
- Acronym / sponsor ID
- GO 21/27
- Conditions
- Running Related Injuries
- Keywords
- validity, reliability, PRO, Patient Outcome Report, Turkish, Adaptation, Running, Injury
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 90 participants (estimated)
- Lead sponsor
- Hacettepe UniversityUniversity, hospital or other
- Study start
- 10 Feb 2021 (estimated)
- Primary completion
- 16 Jan 2022 (estimated)
- Study completion
- 16 Jan 2022 (estimated)
- First posted
- 8 Feb 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose is to perform a scientific study on TURKISH cross-cultural adaptation, validation and the reliability of UWRI
Detailed description
The primary aim of this study is to perform Turkish cross-cultural adaptation, validation and the reliability of UWRI in runners. The secondary aim of this study is investigating injury rate and types among runners.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Target follow-up
- 7 Days
Who may qualify
- Ages
- 14 to 45 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
- Study population
- Runners
Key inclusion criteria (5 listed)
- 14-45 years old female or male
- Participating in running as amateur, recreational, competitional or professional runner
- Being a short, mid, or long distance runner
- Being native Turkish speaker
- Agreed to participate in the research
Key exclusion criteria (4 listed)
- If there is no surgical history related to running injury in the last 12 months
- If have chronic metabolic disease
- Paralympic athletes
- Pregnant and breastfeeding
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| UWRI-TrQuestionnaire | Other | – |
Primary outcome
Validity and reliability
Time frame: 5-7 days
pearson's correlation 2 tailed analysis; >0,60 good, 0,31-0,59 medium, <0,30 bad
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Feb 2021.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Running Related Injuries, 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 5 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: status not confirmed, as of the sponsor's last update on 8 Feb 2021. 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 Elif Turgut (0505 6450049, elifcamci@hacettepe.edu.tr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Validity and reliability (time frame: 5-7 days). 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 8 Feb 2021.