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Clinical Trials/NCT06029556
NCT06029556RecruitingNot Applicable

Effects of Early Mobilization on Functional Capacity, Physical Activity and Kinesiophobia in Post Coronary Artery Bypass Grafting

Riphah International University1 site in 1 country70 target enrollmentStarted: December 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
70
Locations
1
Primary Endpoint
Tampa Scale of Kinesiophobia

Study Overview

Brief Summary

In this study the investigator aim to find the effects of early mobility on different physical activity protocols in post CABG patients. Physical activity, functional status, functional capacity, Kinesiophobia, ICU mortality, heart rate, blood pressure, oxygen saturation, length of hospital stay and sternal instability. To compare the physical activity protocol used by physical therapist.

Detailed Description

Current study will compare two different early mobility protocols and will help in assessing best protocol to be use in cardiac ICU for better outcomes of patients.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Sequential
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
40 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age 40-70 years
  • •Both Genders
  • •Extubated patients with no Complication
  • •Post CABG (Elective)
  • •Vitally stable
  • •Selective CABG surgeries

Exclusion Criteria

  • •Post anesthesia Psychosis
  • •Corrective surgeries
  • •Post CABG Stroke
  • •Infectious wound
  • •Participants with a physical disability
  • •Intra-aortic balloon pump (IABP)

Arms & Interventions

Ergometry in Bed

Experimental

Intervention: Mobility out of Bed (Other)

Mobility out of Bed

Active Comparator

Intervention: Mobility out of Bed (Other)

Mobility out of Bed

Active Comparator

Intervention: Ergometry in Bed (Other)

Ergometry in Bed

Experimental

Intervention: Ergometry in Bed (Other)

Outcomes

Primary Outcomes

Tampa Scale of Kinesiophobia

Time Frame: Pre Operative (Baseline), 1st Assessment (0 Week) and 2nd Assessment (4 week)

Evaluate the fear of movement during activity ,17 items a self-reporting questionnaire based on evaluation of fear of movement, fear of physical activity, and fear avoidance. Individual item scores range from 1-4, with the negatively worded items (4,8,12,16) having a reverse scoring (4-1). The 17 item TSK total scores range from 17 to 68 where the lowest 17 means no or negligible kinesiophobia, and the higher scores indicate an increasing degree of kinesiophobia. Changes will be measured at baseline and at completion of 4th week

BAECK PHYSICAL ACTIVITY QUESTIONNAIRE

Time Frame: Pre Operative (Baseline), 1st Assessment (0 Week) and 2nd Assessment (4 week)

Evaluates the physical activity over the past 12 months. The MBPAQ (BHPAQ) evaluates habitual physical activities in individuals. Activities are scored on a scale of 1-5. A score of 5 indicates the most activity and 1 indicates the least activity for each index.

Functional Status score Questionnaire

Time Frame: Pre Operative (Baseline), 1st Assessment (0 Week) and 2nd Assessment (4 week)

Five item scale measures the physical performance of patients in ICU.The Functional Status Score for the Intensive Care Unit (FSS-ICU) is a 5-item performance-based measure that utilizes an 8 point, ordinal scale to measure physical function for patients in the intensive care unit setting.

6 minute walk Test

Time Frame: Pre Operative (Baseline), 1st Assessment (0 Week) and 2nd Assessment (4 week)

Sub-maximal test evaluates the aerobic endurance. The 6-minute walk test (6MWT) assesses distance walked over 6 minutes as a sub-maximal test of aerobic capacity/endurance.

Secondary Outcomes

  • STERNAL INSTABILITY SCALE:(Pre Operative (Baseline), 1st Assessment (0 Week) and 2nd Assessment (4 week))
  • BORG RATING OF PERCEIVED EXERTION(Pre Operative (Baseline), 1st Assessment (0 Week) and 2nd Assessment (4 week))
  • Length of Hospital stay(Pre Operative (Baseline), 1st Assessment (0 Week) and 2nd Assessment (4 week))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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