The Weighting of the Balance

February 27, 2023 updated by: Gerardo Candoni, Hospital de Rehabilitacion Manuel Rocca

Weighting of Balance Deficiencies Performed by Physical Therapist in Argentina in Subjects With Risk of Falling

Summary Introduction: Falls are involuntary events that cause loss of balance and hit the body on the ground or on another firm surface that stops it. 40% of people with various neurological disorders fall one or more times, and of all these, 21% suffer a fall-related injury. Objective and instrumented gait analysis is an important tool for estimating the risk of falls in patients.

Objective: To describe the protocols used by physical therapist residing in Argentina when categorizing a balance problem within the framework of neurorehabilitation, vestibular rehabilitation, geriatrics and gerontology. Identify the barriers and facilitators self-perceived by physical therapist that make it difficult to weight deficiencies in balance.

Method: An observational, descriptive, cross-sectional study of the online survey type will be carried out. The recommendations given by the Checklist for Reporting of Survey Studies will be used. The survey, which was created by the researchers of this study, will consist of 26 items divided into 4 sections. It will be aimed at all those physical therapist in Argentina who are dedicated to neurorehabilitation, vestibular rehabilitation, geriatrics and gerontology. The type of sampling used will be non-probabilistic by snowball, which will be done online through the SurveyMonkeyTM tool.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Materials and method Study design An observational, descriptive, cross-sectional study will be carried out. For its future report, the recommendations given by the Checklist for Reporting of Survey Studies (CROSS) will be used.

Sample Characteristics All those physical therapist and related degrees dedicated to neurorehabilitation/vestibular rehabilitation/geriatrics and gerontology who practice in Argentina and who have experience in weighing balance deficiencies in subjects at risk of falling will be included. All surveys with missing data will be excluded. The type of sampling used will be non-probabilistic by snowball.

Data collection methods The online type survey which was created by the researchers of this study, will be made up of 25 items divided into 4 sections, a restriction will be created in each item to prevent respondents from leaving it without answering and those who have met all the inclusion criteria will access it.

  • The first section (respondent characteristics) consists of 10 questions.
  • The second section (weighting performed by the respondent) is made up of 12 questions. Those participants who choose the "no" option in question 11 will go on to the next section.
  • The third section (self-perception of barriers and facilitators at the time of weighting) is made up of 2 questions.
  • The fourth section (learning needs) consists of a question. Within the second section, the choice of scales was made based on a previous search in the literature about those that are most used, which to date have not been translated or adapted cross-culturally into Argentine Spanish, most of them. the same It will be aimed at all those physical therapist in Argentina who are dedicated to neurorehabilitation, vestibular rehabilitation, geriatrics and gerontology. With this purpose, a pilot test was carried out prior to the beginning of the study with the objective of the viability and understanding of the survey, it was carried out with 10 experts in the area. They were given a sheet with questions aimed at finding out the difficulties they encountered when answering the survey in general or with a particular question. Modifications were made through consensus among the authors.

Survey Administration You will be invited to participate in the study by sending the survey via email and through social network links (FacebookTM, TwitterTM, InstagramTM, LinkedinTM and WhatsappTM). The invitation will be given to specialized groups in the area, specialization careers, physical therapy colleges in the country and the Argentine association of kinesiology. The invitation will contain the objective of the study and its corresponding link to access the survey, which will be online through the SurveyMonkeyTM tool.

The period in which the current link will be maintained will be 2 months or until the required sample size is reached. To avoid multiple participation of participants, the same tool to be used (SurveyMonkeyTM) prevents double completion when using the same device. In addition, a restriction will be applied to each question, thus preventing them from leaving unanswered answers.

Sample size The required sample size will be 400 participants, since the accepted level of error will be 5%. In turn, an analysis divided by half of the consistency will be carried out, in order to determine if the results obtained are reliable or not.

Study Preparation Prior to the activation of the survey link, contact will be made throughout the previous month in different institutions and experts on the subject, with the aim of increasing the degree of knowledge and interest in it at the time of the start of the study. Contact will be made through emails and different social networks (FacebookTM, TwitterTM and InstagramTM).

Ethical considerations Given the voluntary and anonymous nature of the study, the signature of the informed consent of the participants will not be required, as established by resolution 1480/2011. Before accessing the questionnaire, participants will receive an information sheet that will include study information, investigator contact information, a privacy statement, and a statement regarding voluntary participation. At all times, the protection of the identity and data of the study participants will be preserved, in accordance with current legal regulations National Law on Protection of Personal Data 25326, in accordance with international regulations in accordance with the provisions of the Declaration of Helsinki.

Study Type

Observational

Enrollment (Actual)

205

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Buenos Aires, Argentina, 1079
        • Hospital Rocca

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

23 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Physical therapist in Argentina who are dedicated to neurorehabilitation, vestibular rehabilitation, geriatrics and gerontology who practice in Argentina

Description

Inclusion Criteria:

  • Physical therapist in Argentina who are dedicated to neurorehabilitation, vestibular rehabilitation, geriatrics and gerontology.
  • Practice in Argentina.
  • Have experience in weighing balance deficiencies in subjects at risk of falling

Exclusion Criteria:

• All surveys with missing data will be excluded

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Balance assessment
Time Frame: 2022
It will be measured through the self-report of the respondent whether or not they use a standardized scale or clinical observation with their patients. The variable will be categorized as dichotomous qualitative and the response options will be yes or no.
2022

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2022

Primary Completion (Actual)

January 30, 2023

Study Completion (Actual)

February 28, 2023

Study Registration Dates

First Submitted

March 4, 2022

First Submitted That Met QC Criteria

March 15, 2022

First Posted (Actual)

March 17, 2022

Study Record Updates

Last Update Posted (Estimate)

February 28, 2023

Last Update Submitted That Met QC Criteria

February 27, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 6550

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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