Squat Jump Performance and Chiropractic Ankle Manipulation
The Effects of Chiropractic Ankle Manipulation on Athletic Performance of College-Aged Recreational Athletes: Randomized Controlled Trial
1 other identifier
interventional
60
1 country
1
Brief Summary
The goal of this clinical trial is to learn if chiropractic ankle manipulation can improve squat jump performance. It will also learn about the relationship among chiropractic ankle manipulation, ankle range of motion, and squat jump performance. The main questions it aims to answer are:
- Does chiropractic ankle manipulation increase squat jump height?
- Is there a relationship among chiropractic ankle manipulation, ankle range of motion, and squat jump performance? Researchers will compare squat jump performance between subjects who receive chiropractic ankle manipulations with control subjects to see if ankle chiropractic manipulation works to improve squat jump performance. Participants will:
- Visit the research laboratory for one testing session to measure ankle range of motion and squat jump performance, before and after their randomly assigned intervention arm
- Receive either a chiropractic ankle manipulations or rest quietly as the control condition during the testing session.
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 Jun 2026
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
First Submitted
Initial submission to the registry
May 31, 2026
CompletedStudy Start
First participant enrolled
June 1, 2026
CompletedFirst Posted
Study publicly available on registry
June 11, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
May 1, 2027
June 11, 2026
May 1, 2026
11 months
May 31, 2026
June 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Squat Jump Height
Subjects will be instructed to jump upwards from the starting squat position as high as possible. Subjects will perform 3 to 6 jumps with 3 consecutive jump heights being within 5% of each other to ensure maximum jump height is achieved. There will be a one-minute rest between jumps. * Starting position. Subjects will assume the starting squat position with their hips at 90°, knees at 120°, and ankles at 85° as positioned by the PI. An adjustable plyometric jump box will be used to standardize the starting position. Hands will be resting across their chest with the trunk and head positioned straight ahead. * Squat Jump: Subjects will be instructed to jump as high as possible and land in a comfortable position. Hands will remain across the chest for the duration of The Optojump photoelectric cell system (OptoJump) will be used to record jump height. OptoJump demonstrates strong concurrent validity and excellent test-retest reliability for the estimation of vertical jump height
Baseline on Day 1 to Immediately after Intervention on Day 1
Range of Motion of Ankle Dorsiflexion
Knee-to-wall ankle dorsiflexion test: * Ankle dorsiflexion ROM (distance from wall - cm) is the maximum distance of the big toe from the wall while maintaining contact between the wall and the knee with the heel on the ground. * The subject will repeat the Knee-to-wall ankle dorsiflexion test three times at this maximum distance to allow the PI to record three goniometer measurements of ankle dorsiflexion ROM (degrees°).
Baseline on Day 1 to Immediately after Treatment on Day 1 and at End of Test Session on Day 1
Secondary Outcomes (3)
Leg Muscle Power (W/Kg)
Baseline on Day 1 to Immediately after Intervention on Day 1
Contraction Velocity of Leg Muscles (mm/s), Force-Velocity Curve
Baseline on Day 1 to Immediately after Intervention on Day 1
Rate of Force Development of Leg Muscles (N/s), Slope of the Force - Velocity Curve
Baseline on Day 1 to Immediately after Intervention on Day 1
Study Arms (2)
Chiropractic Ankle Manipulation
EXPERIMENTALLEM - Lower Extremity Manipulation: Subjects assigned to the LEM Intervention Group will receive a short lever, high velocity, low-amplitude distractive (caudal) thrust directed at the talocrural joint. The treating chiropractor will deliver the LEM to the right ankle then the left ankle. LEM is an adjustment for long axis distraction of the tibiotalar joint with the goal to improve dorsiflexion of the ankle joint.
Control
NO INTERVENTIONSubjects assigned to the Control Group will rest quietly, supine (face up), on the chiropractic treatment table for five (5) minutes.
Interventions
The lower extremity manipulation (LEM) procedure is a short lever, high velocity, low-amplitude distractive (caudal) thrust directed at the talocrural joint. The treating chiropractor will deliver the LEM to the right ankle then the left ankle. LEM is an adjustment for long axis distraction of the tibiotalar joint with the goal to improve dorsiflexion of the ankle joint.
Eligibility Criteria
You may qualify if:
- age range from 18 to 35 years old; and
- participating in recreational exercise, three times a week for at least 30 minutes. Recreational exercise includes ball sports (e.g. soccer, basketball, volleyball, etc.), racket sports (e.g. tennis, pickle ball, racket ball, etc.), strength/combat sports (e.g. weight lifting, boxing, martial arts, kickboxing, etc.), endurance sports (running, cycling, rock climbing, etc.), snow/ice sports (downhill or cross-county skiing, snow shoeing, hockey, etc.), interval training (e.g., high-intensity interval training), sprint interval training, repeated sprint training etc.) or moderate-intensity aerobic activities (step classes, dance classes, hiking, etc.)
You may not qualify if:
- professional or amateur ranked athlete;
- acute or chronic musculoskeletal injury / condition of the feet, ankles, knees, and/or hips;
- acute or chronic musculoskeletal injury / condition of the spine;
- pregnancy or there is a possibility of pregnancy.
- any diagnosed medical condition; and
- any prescribed medications with the exceptions of birth control, anxiety, or attention-deficit/hyperactivity disorder (ADHD) medications.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Biomechanics Laboratory at Northeast College of Health Sciences
Seneca Falls, New York, 13148, United States
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dean of Research
Study Record Dates
First Submitted
May 31, 2026
First Posted
June 11, 2026
Study Start
June 1, 2026
Primary Completion (Estimated)
May 1, 2027
Study Completion (Estimated)
May 1, 2027
Last Updated
June 11, 2026
Record last verified: 2026-05