Stabilization Exercises for Young Adults With Habitual Knuckle Cracking
Effects of Stabilization Exercises on Functional Performance, Proprioception, and Joint Laxity in Young Adults With Habitual Knuckle Cracking: A Randomized Controlled Trial
1 other identifier
interventional
42
0 countries
N/A
Brief Summary
Habitual knuckle cracking is a widespread behavior caused by intra-articular pressure changes and gas release in synovial joints; however, its long-term effects on hand sensorimotor function, joint laxity, and overall biomechanics remain debated, with no structured clinical exercise interventions currently established. This prospective, randomized controlled trial aims to evaluate the effectiveness of a 4-week targeted stabilization exercise program focusing on the radiocarpal, metacarpophalangeal (MCP), and proximal interphalangeal (PIP) joints in young adults aged 18 to 30 years with habitual knuckle cracking. Participants are randomly allocated to either an intervention group receiving twice-weekly stabilization training (8 total sessions) or an un-exercised control group. The study hypothesizes that structured joint stabilization exercises will significantly improve wrist and finger joint position sense (proprioception), enhance upper extremity functional performance, and reduce joint laxity compared to the control group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
September 8, 2026
CompletedFirst Posted
Study publicly available on registry
September 11, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 25, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 28, 2027
September 11, 2026
September 1, 2026
5 months
September 8, 2026
September 8, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change from Baseline in Joint Position Sense (JPS) Absolute Error at 4 Weeks
Baseline and 4 weeks
Change from Baseline in Joint Laxity
Baseline and 4 weeks
Secondary Outcomes (2)
Change from Baseline in Upper Extremity Functional Performance using the QuickDASH questionnaire
Baseline and 4 weeks
Change from Baseline in Pain Intensity on Visual Analog Scale (VAS)
Baseline and 4 weeks
Study Arms (2)
Stabilization Exercise Group
EXPERIMENTALNon-Exercise Control Group
NO INTERVENTIONInterventions
A 4-week supervised hand and wrist stabilization exercise program conducted 2 times per week (8 total sessions, 30-45 minutes per session). The protocol targets the radiocarpal (wrist), metacarpophalangeal (MCP), and proximal interphalangeal (PIP) joints. Exercises focus on enhancing joint position sense (proprioception), motor control, isometric and dynamic stabilization, and balanced muscle co-activation around the digits and wrist complex. Progression is individualized based on participant tolerance, maintaining movements within non-painful ranges to prevent joint strain. All sessions are supervised by a physical therapist.
Eligibility Criteria
You may qualify if:
- Age between 18 and 30 years,
- Voluntary agreement to participate and signing the Informed Consent Form following detailed study briefing,
- Willingness to attend all assessment and intervention sessions.
You may not qualify if:
- Having an occupation that requires intensive or repetitive use of the upper extremities and fingers,
- History of prior musculoskeletal injury involving the upper extremity or hand,
- Presence of physical or sensory impairments (such as visual or auditory deficits) that could interfere with study procedures,
- History of congenital or acquired orthopedic, neurological, or rheumatological conditions affecting hand or wrist range of motion and function,
- History of hand or wrist trauma requiring medical, conservative, or surgical management within the past 6 months,
- Presence of active skin lesions in the intervention region, including burns, cellulitis, vesicles, bullae, psoriasis, open or closed wounds, scar tissue, active infection, or malignancy,
- Body Mass Index (BMI) ≥30 or a history of morbid obesity.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Borna Farhoomandlead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- MSc, Physiotherapist
Study Record Dates
First Submitted
September 8, 2026
First Posted
September 11, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
February 25, 2027
Study Completion (Estimated)
March 28, 2027
Last Updated
September 11, 2026
Record last verified: 2026-09