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
1 other identifier
interventional
64
1 country
1
Brief Summary
- 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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable heart-failure
Started Jul 2026
Shorter than P25 for not_applicable heart-failure
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 17, 2026
CompletedFirst Posted
Study publicly available on registry
June 23, 2026
CompletedStudy Start
First participant enrolled
July 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
June 23, 2026
June 1, 2026
5 months
June 17, 2026
June 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Six-minute walk test
The Six-Minute Walk Test (6MWT) is a simple, submaximal test that evaluates functional capacity and exercise capacity in patients with chronic heart failure by measuring the distance walked and estimating peak VO2. It will be performed in a 30-meter corridor, where participants will walk as far as possible in six minutes, with heart rate and oxygen saturation monitored before and after the test. This study tested the validity and reliability of the six-minute walk test (6MWT) in cardiac rehabilitation patients, including those with heart failure.
Baseline and 12 Week
EuroQol 5-Dimension Questionnaire
EuroQol 5-Dimension Questionnaire (EQ-5D): The EuroQol-5 Dimension (EQ-5D) is a questionnaire used to measure quality of life (QoL). It evaluates five key areas: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each area has one question, and responses together describe a person's overall health status. For the 5L, scores range from 5 to 25. A lower score indicates better health, while a higher score indicates greater health problems. Patients rate their overall health TODAY on a vertical scale from 0 (worst imaginable health) to 100 (best imaginable health)
Baseline and 12 week
Study Arms (2)
moderate-intensity aerobic training
ACTIVE COMPARATORHigh-intensity interval training
EXPERIMENTALInterventions
Group A will undergo a moderate-intensity aerobic training program as part of a structured cardiac rehabilitation protocol. The program will be supervised sessions, conducted three times per week for 12 weeks. Each session will include approximately 30 minutes of aerobic exercise performed on a bicycle ergometer at an intensity of 60% of heart rate reserve (HRR)
Group B will perform a high-intensity interval training (HIIT) program designed according to established cardiac rehabilitation protocols. Bicycle ergometer will be used, in which each session will begin with a 10-minute warm-up (lower limb large muscle stretches), followed by intervals performed at 80% of heart rate reserve (HRR) for 3 min, alternating with recovery periods at low intensity 40% of HRR for 3 min. The total exercise duration will be approximately 30 minutes per session, conducted three times weekly for 12 weeks under supervision. Participants will be encouraged to maintain self-directed exercise after the intervention period
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- Unstable Heart failure or myocardial infarction (\< 4 weeks).
- Severe arrhythmias, uncontrolled hypertension, or ongoing chest pain during exercise.
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Riphah International University
Islamabad, Fedral, 44000, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad iqbal Tariq, PhD*
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 17, 2026
First Posted
June 23, 2026
Study Start
July 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
December 1, 2026
Last Updated
June 23, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will not share