- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06891027
Loss of Parental Workforce in Paediatric Fractures
Childhood fractures are frequently encountered in orthopaedic practice. 40-64% of boys and 25-40% of girls have at least one fracture by the age of 16. Children, who are more fragile than adults, usually require additional care support during the treatment process. Labour force statistics have determined that one third of the loss of labour force occurs after musculoskeletal injuries.
When the literature is examined, there are many studies investigating loss of labour force after fractures. It was found that 20% of the patients never returned to work after distal radius fracture and the average loss of labour force was 9.2 weeks. In another study, while the return to work period was 60 days in minor hand injuries, it was reported that the return to work could increase to 360 days in major hand injuries. In another study, the average return to work time in patients aged >50 years with fragility fractures was found to be 20.5 days. The rate of return to work after traumatic spinal fracture was found to be only 38.1%.
In daily practice, the investigators observe that parents frequently do not go to work for child care after child fractures. However, there is no similar study investigating this loss of labour force after pediatric fractures in the literature. In this study, the investigators aimed to investigate the loss of parental labour force (LWL) in conservatively followed pediatric fractures
Study Overview
Status
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Yenimahalle
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Ankara, Yenimahalle, Turkey, 06170
- Ankara Etlik City Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients <18 years of age who underwent plaster splinting for any extremity fracture
Exclusion Criteria:
- Parents of patients aged >18 years
- Parents of patients undergoing surgical treatment
- Parents of patients whose initial diagnosis or follow-up was performed at an external centre
- Patients with one parent not working (patients with one working parent will be excluded)
- Parents of patients who did not want to participate in the study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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pediatric fracture
all paediatric (<18 years) patients presenting with a fracture will be included in the study.
parents of patients presenting with a fracture will be informed about the study and parents who are willing to participate in the study will be included.
parents will be given a form indicating various workforce losses (including housework and social life) at the first application.
this form will be received from the parents at the end of treatment.
study data will be collected on this form.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Loss of Parental Workforce Questionnaire
Time Frame: from first presentation after fracture to the end of treatment (approximately 6 weeks in conservative cases, 3 months in surgical treatments)
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A questionnaire called "Loss of Parental Workforce Questionnaire" will be used to evaluate the parental workforce loss.
Also with this questionnaire the effect of treatment choice (conservative or surgical) to parental workforce loss will be assessed.
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from first presentation after fracture to the end of treatment (approximately 6 weeks in conservative cases, 3 months in surgical treatments)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Children's Return to School Time
Time Frame: from first presentation after fracture to the end of treatment (approximately 6 weeks in conservative cases, 3 months in surgical treatments)
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"Loss of Parental Workforce Questionnaire" will also be used to assess Children's Return to School Time.
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from first presentation after fracture to the end of treatment (approximately 6 weeks in conservative cases, 3 months in surgical treatments)
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AEŞH-BADEK-2024-1169
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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