Effectiveness of Closed Kinetic Chain Exercises in Distal Radius Fracture
The Effectiveness of Closed Kinetic Chain Exercises in Individuals With a Distal Radius Fracture
1 other identifier
interventional
20
1 country
1
Brief Summary
The aim of this study is to evaluate the effectiveness of closed kinetic chain exercises during the physiotherapy and rehabilitation process following the healing of a distal radius fracture. A total of 40 participants aged 40-60 years who were diagnosed with distal radius fractures were randomly assigned to two groups: the conventional physiotherapy (CP) group (n=20) and the closed kinetic chain exercise (CKCE) group (n=20). Participants in the CP group underwent a 6-week standard rehabilitation program consisting of conventional physiotherapy sessions conducted 5 days a week. This program included Ultrasound (US), Transcutaneous Electrical Nerve Stimulation (TENS), wrist joint range of motion exercises, stretching exercises, Digiflex, Powerweb, and dumbbell-based strengthening exercises. In the CKCE group, the same CP program was implemented with the addition of CKCE sessions conducted five days a week for 6 weeks. Outcome measures included joint range of motion assessed using the Goniometer Pro mobile application, functionality evaluated with the Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire, pain intensity measured using the Visual Analog Scale (VAS), and joint position sense assessed through the Active Repositioning Test. CKCE may positively affect joint range of motion, arm functionality, pain, and joint position sense by improving the proprioceptive mechanism in individuals with distal radius fractures.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 6, 2024
CompletedFirst Submitted
Initial submission to the registry
January 31, 2025
CompletedFirst Posted
Study publicly available on registry
February 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 9, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 2, 2025
CompletedApril 4, 2025
April 1, 2025
3 months
January 31, 2025
April 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
JPS testing
Joint position sense (JPS) testing was conducted using a standardized protocol with a goniometer for active wrist position measurement. Participants, seated with their elbow flexed on a table, had their wrist passively moved to 30º extension to memorize the position. With vision occluded, they moved their wrist to full flexion and attempted to reproduce the 30º extension. The reproduced wrist position was recorded, and the difference from the reference angle determined the JPS deficit. A zero value indicated perfect reproduction, while absolute differences reflected the deficit's magnitude. Two trials' mean values were used for analysis.
From enrollment to the end of treatment at 8 weeks
Goniometric Measurement
In this study, the affected shoulder's flexion, extension, abduction, internal rotation, and external rotation angles will be measured using a goniometer-pro application. Reference values will include 0-180 degrees for flexion and abduction, 45 degrees for extension, and 0-90 degrees for internal and external rotation
From enrollment to the end of treatment at 8 weeks
Secondary Outcomes (2)
Visual Analog Scale (VAS)
From enrollment to the end of treatment at 8 weeks
Disabilities of the Arm, Shoulder, and Hand (DASH)
From enrollment to the end of treatment at 8 weeks
Study Arms (2)
conventional physiotherapy (CP) group
ACTIVE COMPARATORParticipants in the first group underwent conventional physiotherapy interventions for 6 weeks, 5 days per week.
closed kinetic chain exercises (CKCE) group
EXPERIMENTALParticipants in the second group received a treatment protocol including closed kinetic chain exercises (CKCE) in addition to conventional physiotherapy interventions.
Interventions
Participants in the first group underwent conventional physiotherapy interventions for 6 weeks, 5 days per week. These interventions included Ultrasound (US), Transcutaneous Electrical Nerve Stimulation (TENS), wrist joint range of motion exercises, stretching exercises, and strengthening exercises using Digiflex, Powerweb, and dumbbells. The number of repetitions and sets of the exercises was adjusted based on the patients' conditions, following a progressive approach. US was applied to the affected wrist for a total of 30 sessions, 5 days a week, once daily, for 6 minutes at an intensity of 1.5 W/cm², using an underwater application method. TENS was administered at a frequency of 100 Hertz for 20 minutes. All participants received manual stretching exercises for wrist flexion, extension, ulnar and radial deviation, supination, and pronation. These stretches were performed by a physiotherapist, with 5 repetitions in each direction, holding the end position for 20 seconds.
Participants in the second group received a treatment protocol that included closed kinetic chain exercises (CKCE) in addition to conventional physiotherapy. CKCE exercises were performed with 15 repetitions each and involved stabilizing a ball between the hand and the wall in different arm positions, rolling it in multiple directions. Participants also performed weight-shifting exercises against a wall and on a table, holding positions for 6 seconds. Additionally, in a crawling position, they moved their unaffected arm diagonally on both a firm surface and a cushion.
Eligibility Criteria
You may qualify if:
- Aged between 40-60 years
- Diagnosed with a distal radius fracture
- Applied to Medipol hospitals after the injury and volunteered to participate in the study
- Patients with good cooperation levels will be included in the study
You may not qualify if:
- Having bilateral distal radius fractures
- Having ulna styloid fractures
- Having other orthopedic, neurological, or rheumatological problems involving the ipsilateral upper extremity
- A history of surgery involving the ipsilateral upper extremity
- Associated injuries such as arterial, nerve, or tendon injuries
- Patients without adequate cooperation will be excluded from the study
- Withdrawal Criteria:
- Missing at least one follow-up
- Development of orthopedic or systemic problems unrelated to the trauma
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- burak meneklead
Study Sites (1)
Burak Menek
Istanbul, Beykoz, 34815, Turkey (Türkiye)
Related Publications (1)
Menek B, Dansuk E. Investigating the effects of closed kinetic chain exercises on joint position sense, functionality, range of motion, and pain in individuals with distal radius fracture: a randomized controlled trial. BMC Sports Sci Med Rehabil. 2025 May 31;17(1):137. doi: 10.1186/s13102-025-01195-2.
PMID: 40450369DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 31, 2025
First Posted
February 6, 2025
Study Start
December 6, 2024
Primary Completion
March 9, 2025
Study Completion
April 2, 2025
Last Updated
April 4, 2025
Record last verified: 2025-04