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More Air - Better Performance - Faster Recovery (IMT)

Primary Purpose

Functional Independence, Respiratory Insufficiency

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Inspiratory muscle training (IMT)
Sponsored by
Central Jutland Regional Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Functional Independence focused on measuring Stroke,, Functioning, Fatigue, Voice volume

Eligibility Criteria

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

Inclusion Criteria:

  • First time brain infarction or brain haemorrhage 0-6 month.
  • Able to give written consent and being cognitive and communicative able to understand and participate in the maximal inspiration pressure test (MIP)
  • Reduced MIP below gender and age specific normal standard

Exclusion Criteria:

  • Diagnosis of myocardial infarction within the last 3 months
  • Significant pulmonary disease (severe COPD), saturation below 90 if having COPD for others saturation below 92
  • Neurological deficits other than stroke
  • Facial palsy that affects proper labial occlusion
  • Dizziness or nausea/vomiting during MIP-testing.

Sites / Locations

  • Regional Hospital Hammel NeurocenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Intervention group

Control group

Arm Description

2 x IMT (5-10 min) 2 times a day 7 days a week for 3 weeks with or without supervision Log-book Conventional neurorehabilitation

Conventional neurorehabilitation

Outcomes

Primary Outcome Measures

Maximal inspiratory pressure (MIP)
Change of MIP assess with the Power Breath. This is an objective measurement to describe the inspiratory capacity. Age specific

Secondary Outcome Measures

Functional Independence Measure (FIM) - both total score ( range from 18 to 126, with higher scores indicating more independence) and motor sub score (max 91)
to assess the degree of changed dependency in daily activities
Fatigue Severity Scale (FSS)
to measure change of fatigue (1-63) higher scores indicating more fatigue affected.
6-minutes walking test
to measure change of endurance
Voice volume
to measure change of voice volume by recording of an a-sound with the App Voice Analyst and to measure Phonation endurance (how long the a-sound last)
Expiratory function
To measure change of Peak expiratory flow (PEF), Forced expiratory volume in 1 second (FEV1), Forced vital capacity (FVC) and FEV1/FVC ratio will be assessed with a peak flow meter (Spirometry device Micro 6300)

Full Information

First Posted
October 28, 2020
Last Updated
August 26, 2021
Sponsor
Central Jutland Regional Hospital
Collaborators
Sygekassernes Helsefond
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1. Study Identification

Unique Protocol Identification Number
NCT04686019
Brief Title
More Air - Better Performance - Faster Recovery
Acronym
IMT
Official Title
"More Air - Better Performance - Faster Recovery": Study Protocol for a Randomised Controlled Trial of the Effect of Inspiratory Muscle Training for Adults Post-stroke
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 15, 2021 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
September 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Central Jutland Regional Hospital
Collaborators
Sygekassernes Helsefond

4. Oversight

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

5. Study Description

Brief Summary
The objective of this study is to investigate i) the effect of 3 weeks IMT to adults post-stroke to maximal inspiratory pressure (MIP) and ii) the effects of 3 weeks IMT to the degree of dependency in activities of daily living, endurance in gait, fatigue, voice volume, phonation endurance, and expiratory function. Methods/Design: Randomised controlled trial (RCT) comparing IMT to conventional neurorehabilitation (usual practise). 80 patients, with reduced maximal inspiration pressure (MIP) hospitalized at a specialized neurorehabilitation hospital in Denmark will be included.
Detailed Description
Background: Stroke results in varying disabilities physical, cognitive, emotional and/or social both in short term and long term. Motor impairments are significantly persistent consequences post-stroke among these are decreased respiratory muscle function, decreased ability to expand thorax and postural dysfunction. These deficits influence the patient's ability in daily activities, fatigue, endurance and quality of life. Inspiratory muscle training (IMT) is training to improve the strength and endurance of diaphragm and the external intercostal muscles. The objective of this study is to investigate i) the effect of 3 weeks IMT to adults post-stroke to maximal inspiratory pressure (MIP) and ii) the effects of 3 weeks IMT to the degree of dependency in activities of daily living, endurance in gait, fatigue, voice volume, phonation endurance, and expiratory function. Methods/Design: Randomised controlled trial (RCT) comparing IMT to conventional neurorehabilitation (usual practise). 80 patients, with reduced maximal inspiration pressure (MIP) hospitalized at a specialized neurorehabilitation hospital in Denmark will be included. The intervention group will add-on IMT sessions exercising at 30 % of MIP. Patients in the intervention group perform 2 sessions a day (One session of IMT with IMT threshold flute consists of 2 times 15 inspirations in normal breathing rhythm (5-10 min)), 7 days a week for 3 weeks. Training can be with or without supervision of physiotherapist.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Functional Independence, Respiratory Insufficiency
Keywords
Stroke,, Functioning, Fatigue, Voice volume

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
External assessor unknown to the participants of the intervention group and control group
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
2 x IMT (5-10 min) 2 times a day 7 days a week for 3 weeks with or without supervision Log-book Conventional neurorehabilitation
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Conventional neurorehabilitation
Intervention Type
Other
Intervention Name(s)
Inspiratory muscle training (IMT)
Intervention Description
IMT and conventional neurorehabilitation - treatment as usual. The intervention group will add-on IMT sessions exercising at 30 % of MIP. MIP is measured by instructing the patient to perform five forceful inspirations against an occluded mouthpiece (Power Breath). The best score is multiplied by 0.3 to determine the resistance. IMT is performed with IMT Threshold flute with the calculated resistance. During the measurement with Power Breath the patient sits straight up and uses nose clip. The patient can receive help to hold the Power Breath if necessary. One session of IMT with IMT threshold flute consists of 2 times 15 inspirations in normal breathing rhythm (5-10 min). Patients in the intervention group perform 2 sessions a day (morning and evening), training is performed prior to a meal, 7 days a week for 3 weeks.
Primary Outcome Measure Information:
Title
Maximal inspiratory pressure (MIP)
Description
Change of MIP assess with the Power Breath. This is an objective measurement to describe the inspiratory capacity. Age specific
Time Frame
Assessed 0-4 days before intervention, 0-4 days after ended intervention assessment and 3 months after ended intervention
Secondary Outcome Measure Information:
Title
Functional Independence Measure (FIM) - both total score ( range from 18 to 126, with higher scores indicating more independence) and motor sub score (max 91)
Description
to assess the degree of changed dependency in daily activities
Time Frame
Assessed 0-4 days before intervention, 0-4 days after ended intervention assessment and 3 months after ended intervention
Title
Fatigue Severity Scale (FSS)
Description
to measure change of fatigue (1-63) higher scores indicating more fatigue affected.
Time Frame
Assessed 0-4 days before intervention, 0-4 days after ended intervention assessment and 3 months after ended intervention
Title
6-minutes walking test
Description
to measure change of endurance
Time Frame
Assessed 0-4 days before intervention, 0-4 days after ended intervention assessment and 3 months after ended intervention
Title
Voice volume
Description
to measure change of voice volume by recording of an a-sound with the App Voice Analyst and to measure Phonation endurance (how long the a-sound last)
Time Frame
Assessed 0-4 days before intervention, 0-4 days after ended intervention assessment and 3 months after ended intervention
Title
Expiratory function
Description
To measure change of Peak expiratory flow (PEF), Forced expiratory volume in 1 second (FEV1), Forced vital capacity (FVC) and FEV1/FVC ratio will be assessed with a peak flow meter (Spirometry device Micro 6300)
Time Frame
Assessed 0-4 days before intervention, 0-4 days after ended intervention assessment and 3 months after ended intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: First time brain infarction or brain haemorrhage 0-6 month. Able to give written consent and being cognitive and communicative able to understand and participate in the maximal inspiration pressure test (MIP) Reduced MIP below gender and age specific normal standard Exclusion Criteria: Diagnosis of myocardial infarction within the last 3 months Significant pulmonary disease (severe COPD), saturation below 90 if having COPD for others saturation below 92 Neurological deficits other than stroke Facial palsy that affects proper labial occlusion Dizziness or nausea/vomiting during MIP-testing.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hanne Pallesen, Post Doc
Phone
004523821365
Email
hannpall@rm.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Simon S Kjeldsen, PhD student
Email
simokjel@rm.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jørgen F Nielsen, Professor
Organizational Affiliation
Hammel Neurorehabilitation and Research Centre, University of Aarhus, Hammel, Denmark
Official's Role
Study Chair
Facility Information:
Facility Name
Regional Hospital Hammel Neurocenter
City
Hammel
ZIP/Postal Code
8450
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hanne Pallesen, post doc
Phone
+4523821365
Email
hannpall@rm.dk
First Name & Middle Initial & Last Name & Degree
Simon S Kjeldsen, post doc
Email
simokjel@rm.dk

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
no plan
Citations:
PubMed Identifier
34454573
Citation
Sorensen SL, Kjeldsen SS, Mortensen SS, Hansen UT, Hansen D, Pedersen AR, Pallesen H. "More air-better performance-faster recovery": study protocol for randomised controlled trial of the effect of post-stroke inspiratory muscle training for adults. Trials. 2021 Aug 28;22(1):575. doi: 10.1186/s13063-021-05551-8.
Results Reference
derived

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More Air - Better Performance - Faster Recovery

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