The effect of inspiratory muscle training on pulmonary function, diaphragm thickness and exercise capacity in patients with acute stroke

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0004523

Enrollment

Registered

2019-12-09

Start date

2020-01-02

Completion date

Unknown

Last updated

2019-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device, Others(Therapeutic exercise) : 1) Inspiratory muscle training -Modified and applied to the protocol of Stefan Tino Kulnik et al. (2015), 5 sets of 10 times with 30&#37

of maximum inspiratory pressure, 1 minute rest between sets, 5 times a week -Every week, the therapist reevaluates and increases resistance based on the protocol of Fry et al. (2007). Resistance prot

41 cm H2O Borg RPE &lt

13 -&gt

Pressure resistance (cm H2O) Increased by 2 Borg RPE 13 to 15 -&gt

Pressure resistance (cm H2O) Increased by 1 Borg RPE &gt

15 -&gt

Pressure resistance (cm H2O) Maintained at same level Borg RPE &gt

17 -&gt

Pressure resistance (cm H2O) Reduced by 2 -Subject’s Baseline MIP Pressure: &gt

Pressure resistance (cm H2O) Increased by 4 Borg RPE 13 to 15 -&gt

Pressure resistance (cm H2O) Increased by 2 Borg RPE &gt

Pressure resistance (cm H2O) Reduced by 2 2) Sham Inspiratory muscle training - 10&#37

intensity of peak inspiratory pressure - 5 sets of 10 times, 1 minute rest between sets, 5 times a week 3) Therapeutic exercise - twice a day for 30 minutes, five times a week for four weeks during

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ? no history of cardiovascular or respiratory problems ? first episode of unilateral stroke with hemiparesis during the previous 2 weaks ? mini mental status evaluation score = 24 ? no facial palsy ? no receptive aphasia ? no prior thoracic or abdominal surgery ? can walk more than 15 m independently without assistive devices

Exclusion criteria

Exclusion criteria: ? use of medications for neuromuscular control or that provoke drowsiness ? Unable to perform tests ? There is an allergic reaction to the ultrasonic gel. ? Those who have participated in a study similar to this study within the last year

Design outcomes

Primary

Measure	Time frame
Pulmonary Function (FVC, FEV1, FEV1/FVC, PImax, PEmax );diaphragm thickness	—

Secondary

Measure	Time frame
Balance ability (Limit of stability);gait ability (10M walking test)	—

Countries

Korea, Republic of

Contacts

Public ContactHaneul Lee

Gachon University

leehaneul84@gmail.com+82-32-820-4335

Outcome results