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NCT06308276Completed

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

Effects of Aerobic Versus Resistance Training on Blood Pressure, Cardiorespiratory Fitness and Quality of Life in Post Percutaneous Coronary Intervention Obese Patients

Source: ClinicalTrials.gov · Last updated 23 Jul 2024

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
50 (actual)
First submitted
4 Mar 2024
Start date
1 Mar 2024
Primary completion date
5 Jun 2024
Lead sponsor
Riphah International University
Diseases
Obesity
NCT number
NCT06308276

What you commit to

  • Study type: Interventional
  • Participants enrolled: 50
  • From 1 Mar 2024 to the primary completion date, 5 Jun 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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

Who the study is looking for

  • 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).

Age in the registry: 40 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sialkot Medical and Physiotherapy Center
Coordinator of this site? Confirm its status
SialkotPakistanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.