Feasibility of a Physiotherapy-led Follow-up Programme in Adult Critical Illness Survivors

Not Applicable

Terminated

• Conditions: Post Intensive Care Unit Syndrome
• Interventions: Other: physiotherapy-led follow-up programme

• Registration Number: NCT04175717
• Lead Sponsor: Kantonsspital Winterthur KSW

Brief Summary

Survivors of critical illness might suffer from ongoing physical, cognitive and emotional impairments after being discharged home. Furthermore, several studies have shown that these patients might have a need for ongoing support. However, up until now, it is not known what the optimal follow-up programme for survivor of critical illness after discharge home should look like or which exact patient population would benefit the most. Due to these reasons, it is important to further investigate, how these patients can be optimally supported to recover from their critical illness.

The primary aim of this study is to assess, whether a physiotherapy-led follow-up programme is feasible in adult survivors of critical illness after discharge home in the county hospital of Winterthur.

Furthermore, the investigators evaluate the influence of this physiotherapy-led follow-up programme on health related quality of life, exercise capacity, general muscle strength, inspiratory muscle strength, anxiety and depression.

All of the anticipated 20 patients will partake in the follow-up programme, which will consist out of a nine weeks exercise programme and four education sessions. During the exercise programme, the patients will exercise twice per week under supervision and once by themselves. The supervised exercise sessions will consist out of a combination of a cardiopulmonary and strength training and the unsupervised session will be a physical activity, which the participants like doing. Furthermore, they will participate in education sessions, where they learn things about the intensive care unit, the post-intensive care syndrome, relaxation techniques and how to carry on with exercising.

The whole study will last about ten months and forms a part of a master thesis.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study First Submitted: 2019-11-07
• Study First Submitted QC: 2019-11-21
• Study First Posted: 2019-11-25
• Study Start: 2020-01-20
• Primary Completion: 2020-03-19
• Study Completion: 2020-05-07
• Status Verified: 2020-09
• Last Update Submitted: 2020-09-02
• Last Update Posted: 2020-09-04

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 3

Inclusion Criteria

• Signed informed consent after being informed
• Adult patient (>18 years), who was treated in the ICU of the county hospital of Winterthur and who was ventilated for longer than 48 hours
• Patient, who received inpatient rehabilitation and then was discharged home

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Exclusion Criteria

• Head or spinal cord injury, leading to neurological deficits
• Receiving palliative care
• Fractures diminishing mobility
• Principal diagnosis of chronic obstructive pulmonary disease (COPD)
• Principal diagnosis of myocardial infarction, heart failure or reanimation
• Principal diagnosis of stroke or cerebral bleeding
• Previous diagnosis of dementia or cognitive impairment
• Inability of the participant to follow the procedures of the study, e.g. due to language problems, psychological disorders, etc.;
• Enrolment of the investigator, his/her family members, employees and other dependent persons

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
physiotherapy-led follow-up programme	physiotherapy-led follow-up programme	-

Primary Outcome Measures

Name	Time	Method
The number of participants, who have completed the nine weeks physiotherapy-led follow-up programme	10 weeks	As part of the feasibility assessment of this physiotherapy-led follow-up programme in the county hospital of Winterthur, it will be assessed, how many participants are able to complete the whole programme.

Secondary Outcome Measures

Name	Time	Method
Exercise capacity	10 weeks	Exercise capacity will be evaluated by the six minute walking test, which is a self-paced walking test to assess submaximal functional exercise capacity. The result will tell us, how many meters the participant could walk in six minutes.
General muscle strength	10 weeks	General muscle strength will be measured by the hand grip test with a Jamar dynamometer. The results will be reported in kilograms.
Inspiratory muscle strength	10 weeks	Inspiratory muscle strength will be evaluated by the CareFusion micro RPM, which measures the maximal inspiratory pressure at the level of the mouth. The results will be reported in centimeter of water.
Anxiety and Depression	10 weeks	Levels of anxiety and depression will be assessed by the hospital anxiety and depression scale (HADS), which is a self-administered questionnaire. It contains 14 items (seven to assess anxiety levels und seven to assess depression levels). Each item can be scored from zero to three, leading to a maximal score of 21. The higher a participants scores, the more likely he is to suffer from anxiety or depression (or both).
Health related quality of life	10 weeks	Health related quality of life will be measured by the EQ-5D L5 self-complete paper version, which is a self-report questionnaire. Th questionnaire contains five dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression), with each five levels (no problems, slight problems, moderate problems, severe problems, and extreme problems). The participants rate themselves in these levels. Additionally, they are also asked to rate their health on a visual analog scale from 0 (worst health you can imagine) to 100 (best health you could imagine).

Trial Locations

Locations (1)

Kantonsspital Winterthur; 🇨🇭 Winterthur, Zürich, Switzerland