Effects of Aerobic Versus Resistance Training in Post Percutaneous Coronary Intervention Obese Patients

NCT06308276 | Completed DMC

• 1 other identifier: REC/RCR&AHS/23/0363
• Study Type: interventional
• Target: 50
• Locations: 1 country
• Sites: 1

Brief Summary

The randomized clinical trial (RCT) endeavors to enroll 50 participants, divided equally into aerobic exercise and resistance exercise groups. The study employs rigorous tools such as blood pressure measurement, SF-36 questionnaire, and the Six-Minute Walk Test (6MWT) to assess VO2max.

Conditions

Cardiovascular Diseases

Keywords

Aerobic Exercise; Angioplasty; Obese Patients; Percutaneous Coronary Intervention; Resistance Training

Outcome Measures

Primary Outcomes (3)

• Blood Pressure

  Blood pressure is a crucial physiological parameter often employed as a data collection tool in research, particularly in studies focused on cardiovascular health and related interventions.

  4 Weeks

• Six Minute Walk Test

  The 6-minute walk test (6MWT) serves as a valuable and widely used data collection tool in research, particularly in studies assessing functional capacity, exercise tolerance, and overall physical performance.

  4 Weeks

• SF 36 Questionnaire

  The Short Form 36 (SF-36) is a widely used health-related quality of life (HRQoL) questionnaire that serves as a comprehensive data collection tool in research studies across various disciplines.

  4 Weeks

Study Arms (2)

Group A

ACTIVE COMPARATOR

Brisk walking, jogging, cycling, or low-impact aerobics

Other: Aerobic Training

Group B

ACTIVE COMPARATOR

Full body resistance exercise targeting major muscle groups, including squats, lunges, chest presses, rows, and core exercises

Other: Resistance Training

Interventions

Aerobic Training OTHER

Aerobic Training: Brisk walking, jogging, cycling, or low-impact aerobics

Group A

Resistance Training OTHER

Resistance Training: Full body resistance exercise targeting major muscle groups, including squats, lunges, chest presses, rows, and core exercises

Group B

Eligibility Criteria

• Age: 40 Years - 60 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• Age: Participants must be between 40 and 60 years old.
• Gender: Male and female both.
• Cardiovascular Status: Post Percutaneous Coronary Intervention (PCI) patients with a documented history of coronary artery disease
• Participants who are at least three months post PCI to ensure stabilization of their cardiovascular condition.
• Obesity: Participants must have a Body Mass Index (BMI) equal to or greater than 30 kg/m², indicating obesity.
• Health Status: Participants should be in stable health condition to participate in moderate physical activities.
• Willingness to Participate: Participants must provide informed consent and be willing to comply with the study protocol, including attending scheduled exercise sessions and follow-up assessments.
• Participants capable of engaging in either aerobic or resistance training, were assessed by a physical activity readiness questionnaire (PAR-Q).

You may not qualify if:

• Participants with severe physical limitations, disabilities, or musculoskeletal disorders that would prevent them from engaging in aerobic and resistance exercises.
• Individuals with a history of substance abuse or current substance abuse issues that might interfere with their ability to participate or adhere to the study protocol.
• Patients with Neurological diseases
• Patients with severe or unstable heart conditions, recent heart attack, or heart failure

Sponsors & Collaborators

• Riphah International University: lead

Study Sites (1)

Sialkot Medical and Physiotherapy Center

Sialkot, Punjab Province, 51310, Pakistan

Location

MeSH Terms

Conditions

Cardiovascular Diseases

Interventions

Resistance Training

Intervention Hierarchy (Ancestors)

Exercise Therapy; Rehabilitation; Aftercare; Continuity of Patient Care; Patient Care; Therapeutics; Physical Therapy Modalities; Physical Conditioning, Human; Exercise; Motor Activity; Movement; Musculoskeletal Physiological Phenomena; Musculoskeletal and Neural Physiological Phenomena

Study Officials

• Muhammad Faizan Hamid, MS-CPPT

  Riphah International University

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: Randomized Clinical Trial

Study Record Dates

• First Submitted: March 4, 2024
• First Posted: March 13, 2024
• Study Start: March 1, 2024
• Primary Completion: June 5, 2024
• Study Completion: June 15, 2024
• Last Updated: July 23, 2024

Record last verified: 2024-07

Data Sharing

• IPD Sharing: Will not share

Locations

PA (1)