- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07278791
Survey-Based Study on Recovery Period Differences in Upper Extremity Injuries Among Indoor Climbers by Treatment Method
A Survey-Based Study on Differences in Recovery Periods of Upper Extremity Injuries Among Indoor Climbers According to Treatment Methods
This study aims to investigate the differences in recovery periods of upper extremity injuries among indoor climbers according to their treatment methods.
The research focuses on comparing the recovery duration, specifically the time to return to climbing, between those who received professional physical therapy and those who relied on self-treatment or other conservative management.
Additionally, this survey-based observational study seeks to explore how individual and training-related factors - such as warm-up duration, climbing frequency, and years of experience - affect the occurrence and recurrence of upper extremity injuries.
Participants will complete an online questionnaire consisting of demographic data, climbing habits, injury characteristics, treatment methods, and recovery outcomes.
The data will be collected anonymously and analyzed to determine whether the type of treatment correlates with faster recovery or reduced reinjury risk.
The findings are expected to provide foundational evidence for developing effective rehabilitation and injury-prevention strategies for indoor climbers, and to guide clinicians and trainers in selecting appropriate treatment approaches for upper extremity injuries.
Study Overview
Status
Conditions
Detailed Description
This cross-sectional survey will recruit indoor climbers aged 18-50 who have experienced upper extremity injuries within the past 12 months.
The questionnaire includes sections on injury site and type (e.g., finger, wrist, elbow, shoulder; tendonitis, ligament injury, or muscle tear), treatment method (self-care, physical therapy, injection, surgery, or rehabilitation exercise), treatment duration, and perceived recovery status.
Statistical analysis will be performed to compare mean recovery periods among treatment groups and to examine correlations with demographic and behavioral factors.
The study was approved by the Institutional Review Board of Sahmyook University (IRB No. 2025-06-034-002).
Results from this research may contribute to improved understanding of injury management and evidence-based rehabilitation for indoor climbers.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Changyong Choi, PT, MPT Candidate
- Phone Number: +82-10-7184-3782
- Email: libetoi2@naver.com
Study Contact Backup
- Name: Seungwon Lee, PhD, PT
- Phone Number: +82-2-3399-1638
- Email: swl@syu.ac.kr
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adults aged 18-50 years.
- Individuals who have participated in indoor climbing within the past 12 months.
- Individuals who have experienced an upper extremity injury (e.g., finger, wrist, elbow, shoulder; tendonitis, ligament injury, muscle tear) during indoor climbing within the past 12 months.
- Individuals who received any form of treatment (self-care, physical therapy, injection, surgery, rehabilitation exercise) for the injury.
- Individuals who can provide informed consent and complete an online questionnaire.
Exclusion Criteria:
- Individuals who underwent major orthopedic surgery or fracture-related surgery unrelated to climbing.
- Individuals who required hospitalization or long-term inpatient treatment (>3 months) due to severe musculoskeletal conditions.
- Individuals currently receiving ongoing treatment for the same injury.
- Individuals with neurological, systemic, or medical conditions that significantly affect musculoskeletal recovery.
- Climbing coaches, professional climbers, or clinicians providing treatment (to avoid expert bias).
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Self-Treatment Group
Participants who treated their upper extremity injury through self-managed care such as rest, cold/heat therapy, taping, or over-the-counter medication.
|
|
Physical Therapy Group
Participants who received professional non-surgical physical therapy, including manual therapy, therapeutic exercise, or extracorporeal shockwave therapy.
|
|
Injection Therapy Group
Participants who received non-surgical injection treatments such as prolotherapy, PRP, or steroid injections for upper extremity injury.
|
|
Surgery/Rehabilitation Group
Participants who underwent surgical or invasive procedures followed by rehabilitation or exercise-based recovery programs.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean Recovery Duration (Weeks) According to Treatment Type
Time Frame: 12 months (retrospective survey)
|
The average number of weeks required for indoor climbers to achieve full recovery and return to climbing after upper extremity injury, compared across treatment types (self-care, physical therapy, injection, surgery/rehabilitation).
|
12 months (retrospective survey)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reinjury Rate Within 12 Months
Time Frame: 12 months
|
Proportion of indoor climbers who experienced a recurrent upper-extremity injury in the same anatomical region within the past 12 months.
|
12 months
|
|
Pain Resolution Duration (Weeks)
Time Frame: 12 months (retrospective survey)
|
Number of weeks required for complete pain resolution after upper-extremity injury, based on participant recall.
|
12 months (retrospective survey)
|
|
Return-to-Climbing Criteria (Self-Reported)
Time Frame: 12 months
|
Self-reported criteria participants used to determine readiness to resume climbing after upper-extremity injury (e.g., full pain resolution, daily activity tolerance, strength recovery).
|
12 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Changyong Choi, PT, MPT Candidate, Sahmyook University
- Study Chair: Seungwon Lee, PhD, PT, Sahmyook University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2025-06-034-002
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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