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Cardiac Rehabilitation With and Without Delorme Technique of Progressive Resisted Exercises in Patients of Post PCI.

Not Applicable
Recruiting
Conditions
Percutaneous CORONARY INTERVENTION
Interventions
Other: Standard Cardiac rehabilitation with Delorme technique
Other: standard cardiac rehabilitation
Registration Number
NCT06460571
Lead Sponsor
Riphah International University
Brief Summary

To find the effect of cardiac rehabilitation program with and without progressive resisted exercises on patients after acute stage of PCI with at least 8 weeks history. It is a randomized clinical trial using convenient sampling technique. Randomly assign participants into two groups: An intervention group receiving Delorme progressive resisted exercise along with cardiac rehab and a control group undergoing standard cardiac rehabilitation alone. In Group A, Delorme technique will involve a 10-repetition max of aerobic and resistance exercises along with cardiac rehab. Seven different exercises will be performed in 3 sets of 10-repetition max. The control group will not be performing any type of training but will undergo cardiac rehab alone. Data will be analyzed using t test and SPSS 21 will be used for data collection. Age group will be from ≥70 years with patient undergoing dyspnea along with recent history of primary diseases. Data will be collected from Bethania Hospital, Sialkot through tools like the 6-minute walk test, Rose Angina questionnaire or settle angina questionnaire, quality of life scale (QOLFS), and Modified Borg dyspnea scale.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
52
Inclusion Criteria
  • Age: ≥ 70 years"
  • "Recent history of PCI due to primary diseases (coronary heart disease, acute myocardial infarction, acute coronary syndrome, acute angina)"
  • "Presence of dyspnea"
  • "First-time PCI
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Exclusion Criteria
  • "Renal failure"
  • Chronic liver disease
  • Chest disease
  • Patient who could not fulfill the questionnaire or cooperate through the performed procedures
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Standard Cardiac rehabilitation with Delorme techniquestandard cardiac rehabilitationThe intervention group will receive Delorme technique along with standard cardiac rehabilitation, involving 10 repetition max of aerobic exercises, resistance exercises of 10 minutes will be given in each training session
standard cardiac rehabilitationstandard cardiac rehabilitationThe control group (Group B) will undergo standard cardiac rehabilitation (outpatient cardiac rehabilitation) which include walking, cycling and strength training which will have 5-10 minutes warm-up followed by training for 30-45 minutes, concluding with cool-down without the Delorme technique.
Standard Cardiac rehabilitation with Delorme techniqueStandard Cardiac rehabilitation with Delorme techniqueThe intervention group will receive Delorme technique along with standard cardiac rehabilitation, involving 10 repetition max of aerobic exercises, resistance exercises of 10 minutes will be given in each training session
Primary Outcome Measures
NameTimeMethod
QUALITY OF LIFE SCALE:baseline and fourth week

"The QOLS was originally a 15-item instrument that measured five conceptual domains of quality of life: material and physical well-being, relationships with other people, social, community and civic activities, personal development and fulfillment, and recreation

MODIFIED BORG DYSPNEA SCALEbaseline and fourth week

The Modified Borg Dyspnea Scale (MBS) is a numerical rating system (0-10) assessing dyspnea during submaximal exercise. Administered with the six-minute walk test (6MWT), a common measure for pulmonary arterial hypertension (PAH), the MBS is consistent within a single session

SETTLE ANGINA QUESTIONNAIREbaseline and fourth week

Settle Angina Questionnaire (SAQ) scale is a disease specific scale is a diabetes specific scale for assessing QOL of CHD patients; have 5 items covering domains; Physical Limitation, Angina Stability, Angina Severity, Treatment Satisfaction and Disease Perception

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Bethania Hospital,

🇵🇰

Sialkot, Punjab, Pakistan

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