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Effects of Exercise During the Acute Phase of Burns

Primary Purpose

Burns

Status
Unknown status
Phase
Phase 2
Locations
Belgium
Study Type
Interventional
Intervention
Exercise
Standard of Care
Sponsored by
Universiteit Antwerpen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Burns focused on measuring Burns, Exercise rehabilitation, Exercise Therapy, Muscle wasting, Hypermetabolism, Insulin resistance

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • ≥10 - ≤80 %TBSA
  • Burn depth: 2nd deep / 3rd degree

Exclusion Criteria:

  • Electrical burn (except flash burns)
  • Associated injury: fracture lower limb
  • Diabetes Mellitus type 1
  • Central neurological/neuromuscular disorders (interfering with assessment/exercise)
  • Cognitive / psychological disorders (interfering with cooperation)
  • Cardiopulmonary disease (interfering with exercise safety)
  • Pregnancy
  • Palliative care

Sites / Locations

  • Ziekenhuis Netwerk Antwerpen StuivenbergRecruiting
  • Militaire Hospitaal Koningin Astrid, Neder-Over-HeembeekRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard of Care

Exercise

Arm Description

Standard of care treatment: - including passive / assisted / active movements, stretching, functional exercise, scar treatment Duration: up to 8 weeks

Standard of care + added exercises Exercise type: resistance and aerobic exercise Resistance Exercise: 3x / week (manual resistance, free weights, machines) Aerobic exercise: 2x / week (cycle ergometer, treadmill) Duration: up to 8 weeks

Outcomes

Primary Outcome Measures

Change in quadriceps muscle layer thickness (QMLT)
Method: B-mode ultrasound on the anterior aspect of the thigh. Technique: maximal and minimal pressure Location: measured at 1/2 and 2/3 of the distance between anterior superior iliac spine and the superior pole of the patella. Analysis: An average of 3 trials will be recorded and analyzed using dedicated software
Change in rectus femoris cross sectional area (RF-CSA)
Method: B-mode ultrasound on the anterior aspect of the thigh. Technique: minimal pressure. Location: measured at the most proximal distance where the entire muscle belly is still visible on the ultrasound image. Analysis: An average of 3 trials will be recorded and analyzed using dedicated software.

Secondary Outcome Measures

Change in insulin resistance
Method: HOMA-2 calculated by fasting plasma glucose and insulin

Full Information

First Posted
August 10, 2020
Last Updated
August 12, 2020
Sponsor
Universiteit Antwerpen
Collaborators
Research Foundation Flanders
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1. Study Identification

Unique Protocol Identification Number
NCT04511104
Brief Title
Effects of Exercise During the Acute Phase of Burns
Official Title
Effects of Exercise During the Acute Phase of Burns: A Multicenter Trial in Belgium
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 4, 2020 (Actual)
Primary Completion Date
April 1, 2022 (Anticipated)
Study Completion Date
April 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universiteit Antwerpen
Collaborators
Research Foundation Flanders

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
BACKGROUND: Postburn changes in whole-body, glucose and protein metabolism are at their peak during the acute phase of severe burns. The resulting metabolic derangements lead to substantial muscle wasting, insulin resistance, which ultimately hampers full recovery and reintegration into society. PURPOSE: This quasi-experimental trial was initiated to investigate the effects of exercise-based rehabilitation on muscle wasting, insulin resistance, and quality of life during the acute phase of severe adult burns. METHODS: Moderate to severely burned adults (10-80%TBSA) will be recruited from two Belgian burn centres. Subjects allocated to the intervention group will undergo an up to 8-week-long exercise program in addition to standard care rehabilitation. As part of the exercise program, participants will carry out progressive resistance and aerobic training, initiated as soon as medical safety and patient cooperation allow. Exercise type and dosage will be chosen according to patient status in terms of grafts, mobility, and strength. The control group will receive standard care rehabilitation only, including passive, assisted, active range of motion exercise, functional exercise, and scar treatment. The effect on muscle wasting will be determined by B-mode ultrasound-derived measures of quadriceps muscle layer thickness (QMLT) and rectus femoris cross sectional area, as well as peak force measurements by handheld dynamometry. Insulin resistance will be derived from the HOMA-2 index based on fasting plasma glucose and insulin. Quality of life will be determined by the EQ-5D-5L and Burn Specific Health Scale-Brief (BSHS-B) questionnaires. The results of this clinical research will provide insight into the effects of exercise on both a fundamental and clinical spectrum.
Detailed Description
The added exercise intervention is initiated in line with the following readiness criteria, which will be checked prior to each training session: Criteria: Mean arterial pressure (MAP) 60 - 110 mmHg Fraction of inspired oxygen (FiO2) <60% Partial pressure of oxygen / fraction of inspired oxygen (PaO2/FiO2) >200 Respiratory rate <40 bpm Positive end expiratory pressure (PEEP) <10 cmH2O No high inotropic doses (Dopamine >10 mcg/kg/min or Nor/adrenaline <0,1 mcg/kg/min) Temp. 36 - 38,5°C Richmond Agitation Sedation Scale (RASS) -2 - +2 Medical Doctor clearance Medical research council (MRC) score lower limbs ≥3 Accordingly, the post burn starting time differs per enrolled subject. Exercises are administered as in-bed exercises or out-of-bed exercises, depending on whether subjects are able and allowed to engage in out-of-bed mobility. Goal exercise intensity for resistance training is set at 60% peak force based on a weekly peak force measurement by hand-held dynamometry, or on a 3 RM in case of out of bed exercises. Goal aerobic exercise intensity is set at 50-75% peak Watts determined by a weekly cycle ergometer or treadmill ramp protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Burns
Keywords
Burns, Exercise rehabilitation, Exercise Therapy, Muscle wasting, Hypermetabolism, Insulin resistance

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Sequential Assignment
Model Description
Trial phase 1: All eligible subjects will be allocated to the intervention group until n=20 has been reached. To reduce staff workload during phase 1, patients will be allocated to the control group if staff capacity (max. 2 patients per full time employed physiotherapist) is saturated. Trial phase 2: When n=20 has been reached in the intervention group, all further eligible patients will be allocated to the control group for the remaining recruitment period.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard of Care
Arm Type
Active Comparator
Arm Description
Standard of care treatment: - including passive / assisted / active movements, stretching, functional exercise, scar treatment Duration: up to 8 weeks
Arm Title
Exercise
Arm Type
Experimental
Arm Description
Standard of care + added exercises Exercise type: resistance and aerobic exercise Resistance Exercise: 3x / week (manual resistance, free weights, machines) Aerobic exercise: 2x / week (cycle ergometer, treadmill) Duration: up to 8 weeks
Intervention Type
Other
Intervention Name(s)
Exercise
Intervention Description
Resistance and aerobic exercise in addition to standard of care rehabilitation
Intervention Type
Other
Intervention Name(s)
Standard of Care
Intervention Description
Standard of care rehabilitation
Primary Outcome Measure Information:
Title
Change in quadriceps muscle layer thickness (QMLT)
Description
Method: B-mode ultrasound on the anterior aspect of the thigh. Technique: maximal and minimal pressure Location: measured at 1/2 and 2/3 of the distance between anterior superior iliac spine and the superior pole of the patella. Analysis: An average of 3 trials will be recorded and analyzed using dedicated software
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Title
Change in rectus femoris cross sectional area (RF-CSA)
Description
Method: B-mode ultrasound on the anterior aspect of the thigh. Technique: minimal pressure. Location: measured at the most proximal distance where the entire muscle belly is still visible on the ultrasound image. Analysis: An average of 3 trials will be recorded and analyzed using dedicated software.
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Secondary Outcome Measure Information:
Title
Change in insulin resistance
Description
Method: HOMA-2 calculated by fasting plasma glucose and insulin
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Other Pre-specified Outcome Measures:
Title
Change in isometric peak force (knee extension)
Description
Method: Hand-held dynamometry (Lafayette instrument Co. Europe, U.K.). Isometric peak fore is measured by a 'make' manoeuvre with a fixation band disallowing movement. Test position: Supine with a fixation band fixed to the hospital bed. Analysis: Best of 3 trials
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Title
Change in isometric peak force (hip flexion)
Description
Method: Hand-held dynamometry (Lafayette instrument Co. Europe, U.K.). Isometric peak fore is measured by a 'make' manoeuvre with a fixation band disallowing movement. Test position: Supine with a fixation band fixed to the hospital bed. Analysis: Best of 3 trials
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Title
Change in isometric peak force (hip extension)
Description
Method: Hand-held dynamometry (Lafayette instrument Co. Europe, U.K.). Isometric peak fore is measured by a 'make' manoeuvre with a fixation band disallowing movement. Test position: Supine with a fixation band fixed to the hospital bed. Analysis: Best of 3 trials
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Title
Change in hand grip strength
Description
Method: Baseline LITE hydraulic dynamometer Analysis: Best of 3 trials
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Title
Change in Burn Specific Health Scale-Brief (BSHS-B)
Description
Burn-specific quality of life, measured by the Burn Specific Health Scale-Brief questionnaire (Dutch and French language version). Total score 152 (0 worst score, 152 best score), consisting of 6 subdomains: 1) Body imagine (36 points) Simple abilities (36 points) Sexuality (24 points) Affect (32 points) Work (16 points) Interpersonal relationship (8 points)
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Title
Change in EQ-5D-5L
Description
Overall quality of life, measured by EQ-5D-5L (Dutch and French language version) Total score: 25 points (0 worst score, 25 best score), consisting of 5 subdomains Mobility (5 points) Self-care (5 points) Usual activities (5 points) pain / discomfort (5 points) Anxiety / Depression (5 points) EQ overall health assessed on a Visual Analogue Scale, Total 0-100 (0 worst, 100 best score)
Time Frame
Baseline - Hospital discharge (max. 8 weeks)
Title
Number of adverse events
Description
Recording of complications during exercise: Graft take, Wound infections, Medical, Cardio-respiratory safety
Time Frame
Baseline - Hospital discharge (max. 8 weeks)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥10 - ≤80 %TBSA Burn depth: 2nd deep / 3rd degree Exclusion Criteria: Electrical burn (except flash burns) Associated injury: fracture lower limb Diabetes Mellitus type 1 Central neurological/neuromuscular disorders (interfering with assessment/exercise) Cognitive / psychological disorders (interfering with cooperation) Cardiopulmonary disease (interfering with exercise safety) Pregnancy Palliative care
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David R Schieffelers
Phone
+3232659177
Email
david.schieffelers@uantwerp.be
First Name & Middle Initial & Last Name or Official Title & Degree
Ulrike Van Daele
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ulrike Van Daele
Organizational Affiliation
University of Antwerp, Faculty of Medicine and Health Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ziekenhuis Netwerk Antwerpen Stuivenberg
City
Antwerp
ZIP/Postal Code
2060
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cynthia Lafaire, Dr.
First Name & Middle Initial & Last Name & Degree
Lieve De Cuyper, Dr.
Facility Name
Militaire Hospitaal Koningin Astrid, Neder-Over-Heembeek
City
Brussels
ZIP/Postal Code
1120
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas Rose, Dr.

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Datasets will be made available upon request.

Learn more about this trial

Effects of Exercise During the Acute Phase of Burns

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