Strengths and Weaknesses of Physiotherapy in the Daily Work of an Intensive Care Unit

March 26, 2025 updated by: Ruben Cuesta Barriuso, University of Oviedo

Strengths and Weaknesses of Physiotherapy in the Daily Work of an Intensive Care Unit: A Qualitative Study

Background. A stay in the Intensive Care Unit can cause long-term problems and physiological changes at the neuromuscular and respiratory levels in critically ill patients. Early physiotherapy in these patients is safe and feasible to avoid or reduce the adverse musculoskeletal and respiratory effects of the stay in this hospital unit.

Objective. To identify the strengths and barriers of Physiotherapy in an Intensive Care Unit, according to the vision of different Health Science professionals.

Method. Qualitative observational study using individual interviews and focus groups. 18 people (6 doctors, 6 nurses and 6 physiotherapists) will be included in the study. The 18 health professionals will participate in personal interviews and focus groups (3 focus groups with 6 participants each). Participants will be recruited from the Intensive Care Unit of the Hospital Universitario Central de Asturias. Data will be analysed using the thematic analysis approach according to Braun and Clarke's method. We will use face-to-face interviews and focus groups to collect data and analyse them through thematic analysis. Purposive sampling will be used to recruit our participants. We will continue to recruit participants, if necessary, until saturation of data from the thematic analysis is reached.

Expected outcomes. To assess the knowledge, perceptions and expectations of the healthcare staff in the Intensive Care Unit regarding Physiotherapy in the management of patients admitted to this Unit. To identify the strengths of Physiotherapy in the management of these patients.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

21

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

    • Asturias
      • Oviedo, Asturias, Spain, 33006
        • University of Oviedo

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

To protect the privacy of the healthcare professionals, we will invite the Heads of Service and Section of the Intensive Care Unit to approach potential participants who, based on their personal and clinical experience, may be able to participate in the study. Subsequently, we will schedule a time for personal interviews and focus groups if potential participants are interested in taking part in the study. With the support of the Intensive Care Unit managers, we will be able to recruit healthcare professionals who meet the selection criteria.

Description

Inclusion Criteria:

  • Professionals from the Intensive Care Unit of the Hospital Universitario Central de Asturias.
  • With clinical experience of at least 2 years.
  • Currently working or having worked in coordination with physiotherapists in the Intensive Care Unit.

Exclusion Criteria:

  • Professionals who are unfamiliar with the usual physiotherapy therapy in an Intensive Care Unit.
  • Resident interns in their first year of training.

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Observacional group
18 people (6 doctors, 6 nurses and 6 physiotherapists) will be included in the study. The 18 health professionals will participate in personal interviews and focus groups (3 focus groups with 6 participants each). Participants will be recruited from the Intensive Care Unit of the Hospital Universitario Central de Asturias.
Following the design of the questionnaire, using open-ended questions based on the availability, accessibility, acceptability and quality (AAAQ) framework, qualitative semi-structured personal interviews were used to collect the data. In this way it was possible to collect information in a more detailed way. The subjects included in the study had to answer the questions posed by the main researcher, responding with open or closed answers, through a questionnaire created for this purpose.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assess the knowledge on Physiotherapy in the Intensive Care Unit
Time Frame: Screening visit
Through open questions focused on the knowledge of physiotherapy in the hospital setting of the Intensive Care Unit: "Are you familiar with the presence of physiotherapists in ICUs?", "Have you previously worked in an ICU that includes physiotherapists?", "Once a patient is admitted to the ICU, when should the physiotherapy intervention start? And when does it actually start?", "What do you think are and should be the functions of physiotherapists in the ICU?", "What do you think are and should be the functions of physiotherapists in the ICU?
Screening visit
Assess the benefits on Physiotherapy in the Intensive Care Unit
Time Frame: Screening visit
Through open questions focused on the benefits of physiotherapy in the hospital environment of the Intensive Care Unit: "What do you think are the benefits for patients of having physiotherapists in the ICU?", "From the point of view of the work of the physiotherapist, what benefits do you consider most important for the patients admitted to the ICU?", "From the point of view of the work of the physiotherapist, what benefits do you consider most important to facilitate multidisciplinary work in the ICU?"
Screening visit
Assess the collaboration between healthcare professionals in the Intensive Care Unit
Time Frame: Screening visit
Through open questions focused on the collaboration between healthcare professionals in the Intensive Care Unit: "Have you experienced any challenges in the collaboration between the professionals involved in ICU care in relation to physiotherapy?", "How do you think multidisciplinary collaboration between healthcare professionals in the ICU and the physiotherapists working in the ICU could be improved?
Screening visit
Assess the needs and recommendations of Physiotherapy in the Intensive Care Unit.
Time Frame: Screening visit
Through open questions focused on the needs and recommendations of Physiotherapy in the Intensive Care Unit: "What additional resources or support do you consider necessary to optimise the presence of physiotherapists in the ICU?", "Do you have any specific recommendations to improve the integration of physiotherapists in the care of patients admitted to the ICU?
Screening visit

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)

May 9, 2024

Primary Completion (Actual)

May 13, 2024

Study Completion (Actual)

March 15, 2025

Study Registration Dates

First Submitted

May 6, 2024

First Submitted That Met QC Criteria

May 8, 2024

First Posted (Actual)

May 9, 2024

Study Record Updates

Last Update Posted (Actual)

April 1, 2025

Last Update Submitted That Met QC Criteria

March 26, 2025

Last Verified

May 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • FisUCI

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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