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NCT06325189Completed

Effects of Aerobic Interval Training on Fatigue Level and Functional Performance in Post Angioplasty Patients

Source: ClinicalTrials.gov · Last updated 22 Mar 2024

Brief summary (registry, in English)

The goal of this randomized controlled trial is to determine the effects of aerobic interval training on levels of tiredness and functional performance in post-angioplasty patients. The main question it aims to answer is: Does aerobic interval training reduce fatigue and improve functional performance compared to medication alone in post-angioplasty patients? Participants will: Be randomly assigned to either the control group (medication) or the experimental group (medication + aerobic interval training) Perform aerobic interval training for 30 minutes, three times a week, for six weeks (experimental group only) Complete pre and post-intervention assessments using the fatigue severity scale, the 6-minute walk test, and the one minute sit to stand test Researchers will compare the two groups to see if aerobic interval training leads to significant improvements in fatigue levels and functional performance.

Status (registry)
Completed
Study type
Interventional
Enrollment
47 (actual)
First submitted
17 Mar 2024
Start date
20 Jul 2023
Primary completion date
1 Dec 2023
Lead sponsor
Riphah International University
NCT number
NCT06325189

What you commit to

  • Study type: Interventional
  • Participants enrolled: 47
  • From 20 Jul 2023 to the primary completion date, 1 Dec 2023
  • 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

  • Patients with neurological disorders
  • Patients with valvular and obstructive airway diseases.
  • Patients with acute infections, malignancy
  • Angioplasty complications such as arrhythmias, blood clots in-stent, and atrial fibrillations
  • Patients with uncontrolled hypertension.
  • Patients with uncontrolled diabetes.

Other

  • Presence of fracture.

Who the study is looking for

  • Patient with post angioplasty (having 1 or 2 stents)
  • Patient who completed phase 1 cardiac rehabilitation
  • Post coronary angioplasty patients 2 weeks of hospital discharge.

Age in the registry: 40 years to 65 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
Gulab Devi Chest Hospital
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

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