Pain Clinical Trial
Official title:
Effect of Different Techniques of Recovery After Fadiga in Para-athletes
Para-athletes are submitted and intense efforts in training and competitions that often overlap in days and weeks. In this sense, and in the search for better brands and indexes, it is necessary to use recovery methods that allow less late muscle pain and better physical performance. Recovery methods are widely used in athletes of various modalities, however there are no studies that point out their effects on para-athletes. This highlights the need for studies on this topic. Paragliding athletes, who train at the Londrina Yacht Club, Londrina Canoeing and Rowing School, who present paraplegia after spinal cord injury, with motor level T10 or lower, without any problem of thermoregulation will participate in the study. All were male and female, with no complaints of musculoskeletal pain or history of upper limb muscle injuries in the last six months and with the same demand for training and competitions. Initially an evaluation will be performed where 1RM, VO2 max, pain, spasticity, body temperature, heart rate variability and electromyographic signal of the involved muscles will be tested. After three days they will be induced to fatigue through a protocol in the traction exercise and immediately directed to one of the 3 intervention groups: ice pack, immersion in cold water or rest. The same baseline evaluations will be repeated after 24, 48 and 72 hours. It is expected that the group submitted to immersion in cold water presents better parameters for pain and sports performance.
Athletes who agree to participate in the study will sign the ICF and will respond to the
questionnaire to characterize the sample. All procedures will be carried out at the Londrina
Canoeing and Rowing School, where athletes are trained.
In the sequence the athlete will be submitted to the test of a maximum repetition (1RM) of
the exercise of traction with the upper limbs, which is specific for canoeing.
This will be performed with the athlete positioned in a decubitus position and well
positioned. In the following, it will be advised to lift the bar with load determined by the
athlete as adequate to carry out the movement, in case of carrying out the movement with ease
and without compensations of other parts of the body the load will increase until the athlete
is no longer able to perform the movement with quality, and then the maximum load determined
as the one in which it was able to perform the complete movement for the last time.
On the first day of collection, the maximum VO2 test will be performed, where the athlete
will perform a test of 8 to 12 minutes where a progressive load will be introduced until the
athlete reaches his maximum oxygen consumption and is no longer able to continue the test.
After three days the athlete will return to the collection site to perform the tests in three
moments:
1. At rest (lying supine on a stretcher):
- HR variability
- VO2
- Resting body temperature
- Assessment of spasticity by the Ashworth scale
- Borg Fatigue Scale.
- EVA
- pressure pain threshold (LDP)
2. During simulation of the paddle on the K1 ergometer (figure 2), which will be held for 6
minutes at comfortable pace, where the last minute data will be used:
- IN G
- VO2
- HR variability After the end of the evaluations, the athlete will be submitted to
the fatigue protocol where he will be guided, to perform the maximum movements of
the traction exercise with load referring to 60% of the 1RM, twice, with interval
of 1 minute between them.
Then it will be taken to another place, near the collection room for randomization, by means
of a draw in a sealed and opaque envelope in one of the three study groups:
- Cold water immersion: The athlete will remain submerged in a "Cryo Control - Ice Bath
Systems®" bathtub, which allows filtration and maintenance of constant water
temperature, and shoulder blade water for 15 minutes in the water at 15 degrees Celsius.
- Ice pack: The athlete will remain for 20 minutes with plastic packets of 500 grams of
ice each, in the region of the evaluated muscles.
- Control: Group in which the athlete will be instructed to remain seated in a comfortable
position, at rest, for 20 minutes.
The randomization and execution of the protocols will be carried out in environments that the
evaluators do not have vision or access, to favor the blindness of the evaluations.
After termination of the intervention protocol, the athlete will be instructed to maintain
routine sleep and feeding activities with the rest of the team, but without participation in
any type of training or physical activity for the next 3 days.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Active, not recruiting |
NCT05559255 -
Changes in Pain, Spasticity, and Quality of Life After Use of Counterstrain Treatment in Individuals With SCI
|
N/A | |
Completed |
NCT04748367 -
Leveraging on Immersive Virtual Reality to Reduce Pain and Anxiety in Children During Immunization in Primary Care
|
N/A | |
Terminated |
NCT04356352 -
Lidocaine, Esmolol, or Placebo to Relieve IV Propofol Pain
|
Phase 2/Phase 3 | |
Completed |
NCT05057988 -
Virtual Empowered Relief for Chronic Pain
|
N/A | |
Completed |
NCT04466111 -
Observational, Post Market Study in Treating Chronic Upper Extremity Limb Pain
|
||
Recruiting |
NCT06206252 -
Can Medical Cannabis Affect Opioid Use?
|
||
Completed |
NCT05868122 -
A Study to Evaluate a Fixed Combination of Acetaminophen/Naproxen Sodium in Acute Postoperative Pain Following Bunionectomy
|
Phase 3 | |
Active, not recruiting |
NCT05006976 -
A Naturalistic Trial of Nudging Clinicians in the Norwegian Sickness Absence Clinic. The NSAC Nudge Study
|
N/A | |
Completed |
NCT03273114 -
Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain
|
N/A | |
Enrolling by invitation |
NCT06087432 -
Is PNF Application Effective on Temporomandibular Dysfunction
|
N/A | |
Completed |
NCT05508594 -
Efficacy and Pharmacokinetic-Pharmacodynamic Relationship of Intranasally Administered Sufentanil, Ketamine, and CT001
|
Phase 2/Phase 3 | |
Recruiting |
NCT03646955 -
Partial Breast Versus no Irradiation for Women With Early Breast Cancer
|
N/A | |
Active, not recruiting |
NCT03472300 -
Prevalence of Self-disclosed Knee Trouble and Use of Treatments Among Elderly Individuals
|
||
Completed |
NCT03678168 -
A Comparison Between Conventional Throat Packs and Pharyngeal Placement of Tampons in Rhinology Surgeries
|
N/A | |
Completed |
NCT03931772 -
Online Automated Self-Hypnosis Program
|
N/A | |
Completed |
NCT03286543 -
Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System
|
N/A | |
Completed |
NCT02913027 -
Can We Improve the Comfort of Pelvic Exams?
|
N/A | |
Terminated |
NCT02181387 -
Acetaminophen Use in Labor - Does Use of Acetaminophen Reduce Neuraxial Analgesic Drug Requirement During Labor?
|
Phase 4 | |
Recruiting |
NCT06032559 -
Implementation and Effectiveness of Mindfulness Oriented Recovery Enhancement as an Adjunct to Methadone Treatment
|
Phase 3 | |
Active, not recruiting |
NCT03613155 -
Assessment of Anxiety in Patients Treated by SMUR Toulouse and Receiving MEOPA as Part of Their Care
|