Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06200493
Other study ID # 2023-10
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 20, 2023
Est. completion date February 28, 2024

Study information

Verified date January 2024
Source Swiss Paraplegic Research, Nottwil
Contact Fabian Ammann, MSc
Phone +41 41 939 66 24
Email fabian.amman@paraplegie.ch
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to learn about the relation between grip position and maximal strength and power in wheelchair rugby and basketball athletes. The main question is to investigate the relationship between maximal isometric force, acceleration, and sprint time. Participants will - pull in their sport wheelchair against a force transducer - push in their sport wheelchair from a force transducer - accelerate as fast as possible with one push - accelerate as fast as possible over a distance of 20m Researchers will compare the wheelchair basketball against wheelchair rugby players to see if there is a difference in the parameters.


Description:

The study duration is approximately 2 hours per participant. First, the screening will be done and the participant does a warmup (~30 min). After that, the participant gets ready for testing, which will last for approximately 90 minutes. In each test, the participants have trial rounds to familiarize with the test procedure. The testing consist of three different exercises, the isometric strength test (IsoMST), the maximum initial push propulsion (MIPP) and the sprint. In the IsoMST a pull setup which was already used in literature and a push setup which has yet to be validated will be used. For the pull setup, the chair of the athlete is fixated on the wall which results in a static situation and allows for an isometric effort. For the push setup, a bumper is installed on the wall, against which the athletes can push with their chair. Different grip position will be measured. In the MIPP test the participants are instructed to accelerate as quickly as possible from standstill with only one push on the rim. The MIPP will be executed with several different grip positions, equal to the IsoMST. For the sprint, 20m will be marked out on a playing court. The athletes are instructed to complete the distance as quickly as possible. Several split times as well as the total time will be measured.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date February 28, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - squad members or doing more than 3h per week wheelchair basket/rugby training - adequately informed and consent confirmed per signature Exclusion Criteria: - Pregnancy based on anamnesis - acute illness, injury, infection, etc., which would impact the measurements.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Swiss Paraplegic Centre Nottwil Lucerne

Sponsors (1)

Lead Sponsor Collaborator
Swiss Paraplegic Research, Nottwil

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Other rate of force development The rate of force development (RFD) in the isometric push and pull test during the first second of maximal push
Other sprint distance time The time for the linear sprint over sub distance in the sport wheelchair during 5 seconds of the linear sprint
Other one push maximal speed The maximal speed reached with one push in the sport wheelchair during the last second of acceleration
Primary maximal pull force The maximal isometric force produced during pulling in the sport wheelchair during 1 second of maximal pulling
Secondary maximal push force The maximal isometric force produced during pushing in the sport wheelchair during the first second of maximal pushing
Secondary maximal acceleration The maximal acceleration reached with one push in the sport wheelchair during the first second of acceleration
Secondary sprint time The time for the linear sprint over 20m in the sport wheelchair during the last second of the 20 metre sprint
See also
  Status Clinical Trial Phase
Active, not recruiting NCT06321172 - Muscle and Bone Changes After 6 Months of FES Cycling N/A
Completed NCT03457714 - Guided Internet Delivered Cognitive-Behaviour Therapy for Persons With Spinal Cord Injury: A Feasibility Trial
Recruiting NCT05484557 - Prevention of Thromboembolism Using Apixaban vs Enoxaparin Following Spinal Cord Injury N/A
Suspended NCT05542238 - The Effect of Acute Exercise on Cardiac Autonomic, Cerebrovascular, and Cognitive Function in Spinal Cord Injury N/A
Recruiting NCT05503316 - The Roll of Balance Confidence in Gait Rehabilitation in Persons With a Lesion of the Central Nervous System N/A
Not yet recruiting NCT05506657 - Early Intervention to Promote Return to Work for People With Spinal Cord Injury N/A
Recruiting NCT04105114 - Transformation of Paralysis to Stepping Early Phase 1
Recruiting NCT03680872 - Restoring Motor and Sensory Hand Function in Tetraplegia Using a Neural Bypass System N/A
Completed NCT04221373 - Exoskeletal-Assisted Walking in SCI Acute Inpatient Rehabilitation N/A
Completed NCT00116337 - Spinal Cord Stimulation to Restore Cough N/A
Completed NCT03898700 - Coaching for Caregivers of Children With Spinal Cord Injury N/A
Recruiting NCT04883463 - Neuromodulation to Improve Respiratory Function in Cervical Spinal Cord Injury N/A
Active, not recruiting NCT04881565 - Losing Balance to Prevent Falls After Spinal Cord Injury (RBT+FES) N/A
Completed NCT04864262 - Photovoice for Spinal Cord Injury to Prevent Falls N/A
Recruiting NCT04007380 - Psychosocial, Cognitive, and Behavioral Consequences of Sleep-disordered Breathing After SCI N/A
Active, not recruiting NCT04544761 - Resilience in Persons Following Spinal Cord Injury
Completed NCT03220451 - Use of Adhesive Elastic Taping for the Therapy of Medium/Severe Pressure Ulcers in Spinal Cord Injured Patients N/A
Terminated NCT03170557 - Randomized Comparative Trial for Persistent Pain in Spinal Cord Injury: Acupuncture vs Aspecific Needle Skin Stimulation N/A
Recruiting NCT04811235 - Optical Monitoring With Near-Infrared Spectroscopy for Spinal Cord Injury Trial N/A
Recruiting NCT04736849 - Epidural and Dorsal Root Stimulation in Humans With Spinal Cord Injury N/A