Functional StatusNCT05318664
Effects of Cryotherapy on Upper Limb Balance Test
A study testing Cryotherapy in people with Functional Status and Muscle Tone, run by Flávia Carvalho.
Trial summary
The shoulder joint is commonly used and also stricken by high loads and injuries in sports. One technique in emphasis is cryotherapy, a physiotherapeutical intervention characterized by the use of low temperatures for tissue trauma's rehabilitation. Read more about this study
- Who is it for?
- Ages 18 to 28 yearsHealthy volunteers can take part
- Conditions the study is for
- Functional Status, Muscle Tone
- What is being tested?
- Cryotherapy
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- No sites listed yet
- Study dates
- 25 Apr 2022to Jun 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 28 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- 18 to 28 years old
- healthy
- no musculoskeletal complaints
Who cannot join
- failure to follow protocol
- complaints of injury or pain during the assessments
Trial locations and contacts
No sites are listed yet.
About this study
Official title: Effects of Cryotherapy on Upper Limb Balance Test: Randomized Clinical Trial
The shoulder joint is commonly used and also stricken by high loads and injuries in sports. One technique in emphasis is cryotherapy, a physiotherapeutical intervention characterized by the use of low temperatures for tissue trauma's rehabilitation. Several studies analysed the effects of cryotherapy and brought important results related to pain and strength reduction, also to muscle contraction speed reduction. Although, considering the risk-benefit from de intervention it's pertinent to observe the presence of deleterious effects, especially the ones that impact on motor function. This scenario has been brought by scientists and currently the main gap from this theme resides on the repercussions of the technique application on functional answers
Read the detailed description
Eighty participants will receive control (rest) and the experimental condition (cryotherapy), with an interval of 48 hours. The intervention group will undergo: i) assessment, ii) 20 minutes of cryotherapy, iii) reassessment, iv) 20 minutes of rest and v) reassessment, while the control group remains at rest for 20 minutes. Assessments will be composed of shoulder function by the upper quarter y balance test, muscle tone by the myoton pro, skin temperature by a thermographic camera, thermic comfort, perception of balance and beliefs in cryotherapy. Data will be described using mean and standard deviation and compared by Mixed ANOVA (time x intervention) with post Bonferroni tests, with significance level of 0.05.
- Conditions
- Functional Status, Muscle Tone
- Being tested
- Cryotherapy
- Keywords
- shoulder, cryotherapy, balance
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
CryotherapyOther
20 minutes of cryotherapy on the dominant shoulder with ice bags
| Study group | Role | What they receive |
|---|---|---|
| Cryotherapy | Experimental | 20 minutes of cryotherapy on the dominant shoulder with ice bags Receives: Other: Cryotherapy |
| Control | No intervention | 20 minutes of rest |
What is being measured
The primary outcome is the main question the study is designed to answer.
modified Upper Quarter Y Balance Test - mUQYBT)
test for measuring upper extremity reach distance while in a closed-chain position
Measured: Change from baseline to 20 minutes
modified Upper Quarter Y Balance Test - mUQYBT)
test for measuring upper extremity reach distance while in a closed-chain position
Measured: Change from baseline to 40 minutes
Secondary outcomes (15)
Skin temperature
thermographic camera FLIR E-8 XT (FLIR Systems, Sweden)
Measured: Change from baseline to 20 minutes
Skin temperature
thermographic camera FLIR E-8 XT (FLIR Systems, Sweden)
Measured: Change from baseline to 25 minutes
Skin temperature
thermographic camera FLIR E-8 XT (FLIR Systems, Sweden)
Measured: Change from baseline to 30 minutes
Skin temperature
thermographic camera FLIR E-8 XT (FLIR Systems, Sweden)
Measured: Change from baseline to 35 minutes
Skin temperature
thermographic camera FLIR E-8 XT (FLIR Systems, Sweden)
Measured: Change from baseline to 40 minutes
Thermic comfort
a 10cm scale ranging from 0 "very comfortable" and 10 "very uncomfortable" will be used
Measured: Change from baseline to 20 minutes
Thermic comfort
a 10cm scale ranging from 0 "very comfortable" and 10 "very uncomfortable" will be used
Measured: Change from baseline to 40 minutes
Balance perception
a likert scale will be used to answer the question " How good was your balance over the test?" 1=nothing, 2=a little, 3=moderate, 4= a lot, 5=extremely
Measured: Change from baseline to 20 minutes
Balance perception
a likert scale will be used to answer the question " How good was your balance over the test?" 1=nothing, 2=a little, 3=moderate, 4= a lot, 5=extremely
Measured: Change from baseline to 40 minutes
Muscle tone
Muscle tone will be measured in hertz by the MyotonPRO wich has a probe that will be placed perpendicular to the skin surface on the muscle belly previously marked with a pen by the evaluator at the Deltoid;
Measured: Change from baseline to 20 minutes
Muscle tone
Muscle tone will be measured in hertz by the MyotonPRO probe will be placed perpendicular to the skin surface on the muscle belly previously marked with a pen by the evaluator at the Deltoid;
Measured: Change from baseline to 25 minutes
Muscle tone
Muscle tone will be measured in hertz by the MyotonPRO probe will be placed perpendicular to the skin surface on the muscle belly previously marked with a pen by the evaluator at the Deltoid;
Measured: Change from baseline to 30 minutes
Muscle tone
Muscle tone will be measured in hertz by the MyotonPRO probe will be placed perpendicular to the skin surface on the muscle belly previously marked with a pen by the evaluator at the Deltoid;
Measured: Change from baseline to 35 minutes
Muscle tone
Muscle tone will be measured in hertz by the MyotonPRO probe will be placed perpendicular to the skin surface on the muscle belly previously marked with a pen by the evaluator at the Deltoid;
Measured: Change from baseline to 40 minutes
Beliefs
The participants will respond yes or no to the questions "Do you believe that cryotherapy is an effect treatment for acute injuries?" and "Do you believe cryotherapy have deleterious effects on muscle function?"
Measured: Baseline
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Apr 2022
- Study start25 Apr 2022 (estimated)
- Primary completionJun 2022 (estimated)
- Study completionJun 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Functional StatusStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Flávia Carvalho
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Flávia Carvalho, São Paulo State University
- Investigators
- Carlos M Pastre, Study director, São Paulo State University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05318664
- Sponsor's protocol ID
- EC001
- Status last verified
- Apr 2022
- First submitted
- 22 Mar 2022
- Last updated
- 8 Apr 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 Apr 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Cryotherapy on Upper Limb Balance Test: Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT05318664
- Acronym / sponsor ID
- EC001
- Conditions
- Functional Status, Muscle Tone
- Keywords
- shoulder, cryotherapy, balance
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Flávia CarvalhoUniversity, hospital or other
- Study start
- 25 Apr 2022 (estimated)
- Primary completion
- Jun 2022 (estimated)
- Study completion
- Jun 2022 (estimated)
- First posted
- 8 Apr 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The shoulder joint is commonly used and also stricken by high loads and injuries in sports. One technique in emphasis is cryotherapy, a physiotherapeutical intervention characterized by the use of low temperatures for tissue trauma's rehabilitation. Several studies analysed the effects of cryotherapy and brought important results related to pain and strength reduction, also to muscle contraction speed reduction. Although, considering the risk-benefit from de intervention it's pertinent to observe the presence of deleterious effects, especially the ones that impact on motor function. This scenario has been brought by scientists and currently the main gap from this theme resides on the repercussions of the technique application on functional answers
Detailed description
Eighty participants will receive control (rest) and the experimental condition (cryotherapy), with an interval of 48 hours. The intervention group will undergo: i) assessment, ii) 20 minutes of cryotherapy, iii) reassessment, iv) 20 minutes of rest and v) reassessment, while the control group remains at rest for 20 minutes. Assessments will be composed of shoulder function by the upper quarter y balance test, muscle tone by the myoton pro, skin temperature by a thermographic camera, thermic comfort, perception of balance and beliefs in cryotherapy. Data will be described using mean and standard deviation and compared by Mixed ANOVA (time x intervention) with post Bonferroni tests, with significance level of 0.05.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Cryotherapy | Experimental | Other: Cryotherapy20 minutes of cryotherapy on the dominant shoulder with ice bags |
| Control | No intervention | –20 minutes of rest |
Who may qualify
- Ages
- 18 to 28 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- 18 to 28 years old
- healthy
- no musculoskeletal complaints
Key exclusion criteria (2 listed)
- failure to follow protocol
- complaints of injury or pain during the assessments
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Cryotherapy20 minutes of cryotherapy on the dominant shoulder with ice bags | Other | Cryotherapy |
Primary outcome
modified Upper Quarter Y Balance Test - mUQYBT)
Time frame: Change from baseline to 20 minutes
test for measuring upper extremity reach distance while in a closed-chain position
modified Upper Quarter Y Balance Test - mUQYBT)
Time frame: Change from baseline to 40 minutes
test for measuring upper extremity reach distance while in a closed-chain position
15 secondary outcomes
Skin temperature
Time frame: Change from baseline to 20 minutes
Skin temperature
Time frame: Change from baseline to 25 minutes
Skin temperature
Time frame: Change from baseline to 30 minutes
Skin temperature
Time frame: Change from baseline to 35 minutes
Skin temperature
Time frame: Change from baseline to 40 minutes
Thermic comfort
Time frame: Change from baseline to 20 minutes
Thermic comfort
Time frame: Change from baseline to 40 minutes
Balance perception
Time frame: Change from baseline to 20 minutes
Balance perception
Time frame: Change from baseline to 40 minutes
Muscle tone
Time frame: Change from baseline to 20 minutes
Muscle tone
Time frame: Change from baseline to 25 minutes
Muscle tone
Time frame: Change from baseline to 30 minutes
Muscle tone
Time frame: Change from baseline to 35 minutes
Muscle tone
Time frame: Change from baseline to 40 minutes
Beliefs
Time frame: Baseline
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Apr 2022.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Carlos M Pastre study director
São Paulo State University
Questions about this trial
What is this clinical trial studying?
A study testing Cryotherapy in people with Functional Status and Muscle Tone, run by Flávia Carvalho.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 8 Apr 2022. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Flávia A Carvalho (+5518997443624, fla.acarvalho@hotmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
modified Upper Quarter Y Balance Test - mUQYBT) (time frame: Change from baseline to 20 minutes). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Apr 2022.