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NCT07662876Not yet recruiting

Moderate Intensity vs High Intensity Interval Training in Women With Heart Failure

Effects of Moderate Intensity Exercise vs High Intensity Interval Training on Functional Capacity and Quality of Life in Women With Heart Failure

Source: ClinicalTrials.gov · Last updated 23 Jun 2026

Brief summary (registry, in English)

* To determine the effects of moderate intensity exercise vs high intensity interval training on functional capacity in women with heart failure * To determine the effects of moderate intensity exercise vs high intensity interval training on quality of life in women with heart failure

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
64 (estimated)
First submitted
17 Jun 2026
Start date
Jul 2026
Primary completion date
Dec 2026
Lead sponsor
Riphah International University
NCT number
NCT07662876

What you commit to

  • Study type: Interventional
  • Planned participants: 64
  • From Jul 2026 to the primary completion date, Dec 2026
  • 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 design.

Who cannot take part

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

Other illness

  • Unstable Heart failure or myocardial infarction (\< 4 weeks).
  • Severe arrhythmias, uncontrolled hypertension, or ongoing chest pain during exercise.

Other

  • Orthopedic, neurological, or cognitive limitations preventing safe exercise participation.
  • Any medical contraindication to exercise testing.
  • Refusal or inability to provide informed consent or comply with the rehabilitation program.

Who the study is looking for

  • Women aged 40-70 years, diagnosed with Stable Heart Failure (NYHA class II or III).
  • Clinically stable patients referred for exercise-based cardiac rehabilitation by the physician.
  • Able to perform exercise testing (able to walk 150 meters on the six-minute walk test) before starting the program.
  • Women willing to participate and provide informed consent.

Age in the registry: 40 years to 70 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Riphah International University
Coordinator of this site? Confirm its status
IslamabadPakistanUnknown status

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