Ignite Creation Date:
2024-10-26 @ 3:37 PM
Last Modification Date:
2024-10-26 @ 3:37 PM
Study NCT ID:
NCT06551714
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-02-19
Brief Title:
The Effect of Neurophysiological Facilitation Techniques on Health Parameters in Early Stages After Open Heart Surgery
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Effect of Neurophysiological Facilitation Techniques on Pulmonary Function Respiratory Muscle Strength and Functional Capacity in The Early Stage After Open Heart Surgery
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
In this study researchers aimed to investigate effects of neurophysiological facilitation on functional capacity and respiratory parameters of patients who underwent open heart surgery
Do neurophysiological facilitation techniques improve individuals respiratory parameters more than phase 1 cardiac rehabilitation
Do neurophysiological facilitation techniques improve individuals functional capacity more than phase 1 cardiac rehabilitation
Researchers will apply phase 1 cardiac rehabilitation to both groups to see the effectiveness of neurophysiological facilitation techniques
Do neurophysiological facilitation techniques improve individuals respiratory parameters more than phase 1 cardiac rehabilitation
Do neurophysiological facilitation techniques improve individuals functional capacity more than phase 1 cardiac rehabilitation
Researchers will apply phase 1 cardiac rehabilitation to both groups to see the effectiveness of neurophysiological facilitation techniques
Detailed Description:
In this study researchers aimed to investigate effects of neurophysiological facilitation on functional capacity and respiratory parameters of patients who underwent open heart surgery
The study was performed on 32 patients who underwent open heart surgery Patients divided into two groups which study group n18 and control group n14
Range of motion breathing and mobilization exercises within the scope of phase 1 cardiac rehabilitation program were applied to the control group in addition to the phase 1 cardiac rehabilitation program neurophysiological facilitation techniques perioral stimulation intercostal tension anterior basal lift vertebral pressure moderate manual pressure and abdominal co-contraction were applied to the study group
Sociodemographic features and disease-specific findings were recorded on the first postoperative day
Vital signs functional capacity pulmonary function fatigue and dyspnea of every patient were recorded before and after each treatment on the first four postoperative days
Functional capacity was evaluated using Timed Up and Go TUG test and 2-Minutes Walking test 2MWT Pulmonary function was examined using a peak flow meter and respiratory muscle strength was measured using an intraoral pressure measurement device In addition fatigue and dyspnea perception was measured using Modified Borg Scale
Before the first day treatment and after the last day treatment of the four-day treatment patients fatigue severity were assessed with using Fatigue Severity Scale FSS anxiety and depression level with using Hospital Anxiety Depression Scale HADS fear of movement with using TAMPA Kinesiophobia Scale and life quality with using the Minnesota Heart Failure Questionnaire
Before each treatment chest circumference measurements were taken and the perceived pain severity was recorded using Visual Analog Scale VAS
The study was performed on 32 patients who underwent open heart surgery Patients divided into two groups which study group n18 and control group n14
Range of motion breathing and mobilization exercises within the scope of phase 1 cardiac rehabilitation program were applied to the control group in addition to the phase 1 cardiac rehabilitation program neurophysiological facilitation techniques perioral stimulation intercostal tension anterior basal lift vertebral pressure moderate manual pressure and abdominal co-contraction were applied to the study group
Sociodemographic features and disease-specific findings were recorded on the first postoperative day
Vital signs functional capacity pulmonary function fatigue and dyspnea of every patient were recorded before and after each treatment on the first four postoperative days
Functional capacity was evaluated using Timed Up and Go TUG test and 2-Minutes Walking test 2MWT Pulmonary function was examined using a peak flow meter and respiratory muscle strength was measured using an intraoral pressure measurement device In addition fatigue and dyspnea perception was measured using Modified Borg Scale
Before the first day treatment and after the last day treatment of the four-day treatment patients fatigue severity were assessed with using Fatigue Severity Scale FSS anxiety and depression level with using Hospital Anxiety Depression Scale HADS fear of movement with using TAMPA Kinesiophobia Scale and life quality with using the Minnesota Heart Failure Questionnaire
Before each treatment chest circumference measurements were taken and the perceived pain severity was recorded using Visual Analog Scale VAS
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None