NCT07662876

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
64

participants targeted

Target at P25-P50 for not_applicable heart-failure

Timeline
4mo left

Started Jul 2026

Shorter than P25 for not_applicable heart-failure

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Study Progress20%
Jul 2026Dec 2026

First Submitted

Initial submission to the registry

June 17, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

June 23, 2026

Completed
8 days until next milestone

Study Start

First participant enrolled

July 1, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

June 23, 2026

Status Verified

June 1, 2026

Enrollment Period

5 months

First QC Date

June 17, 2026

Last Update Submit

June 17, 2026

Conditions

Keywords

Heart failureModerate IntensityHigh Intensity Interval Training

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 COMPARATOR
Other: moderate-intensity aerobic training

High-intensity interval training

EXPERIMENTAL
Other: High-intensity interval training

Interventions

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)

moderate-intensity aerobic training

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

High-intensity interval training

Eligibility Criteria

Age40 Years - 70 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailswomen with Heart failure
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Heart Failure

Interventions

High-Intensity Interval Training

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

Physical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Muhammad iqbal Tariq, PhD*

    Riphah International University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Muhammad Iqbal Tariq

CONTACT

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

Locations