Trials / Not Yet Recruiting
Not Yet RecruitingNCT07350941
Impact of Cardiac Rehabilitation Adapted for Patients With Heart Failure
RAP-IC Study: Impact of Cardiac Rehabilitation Adapted for Patients With Heart Failure
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 114 (estimated)
- Sponsor
- Puerta de Hierro University Hospital · Academic / Other
- Sex
- All
- Age
- 65 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to evaluate whether a tailored cardiac rehabilitation program, initiated during hospitalization and continued after discharge, can improve functional capacity, mobility, and quality of life in patients over 65 years old with heart failure.
Detailed description
If you meet the inclusion criteria and wish to participate, an initial assessment of your clinical and functional status will be conducted during your hospital stay. A computer system will then randomly assign you to one of the following groups: Cardiac Rehabilitation Group (treatment group): You will participate in a mild exercise program during hospitalization (Phase I), including mobility and respiratory exercises adapted to your clinical condition. After discharge, you will enter a structured in-person cardiac rehabilitation program (Phase II) lasting 3 months, consisting of two 1-hour exercise sessions per week (aerobic, strength, inspiratory, and proprioceptive exercises) plus one weekly educational session. Usual Care Group (control group): You will receive standard recommendations for physical activity and general care. At the end of the study, a final consultation will be conducted to assess differences between the two groups in functional capacity and quality of life.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Cardiac rehabilitation program | Cardiac rehabilitation program, in which patients will attend in person twice weekly (Mondays and Wednesdays or Tuesdays and Thursdays), in groups of up to 8 patients, for 1-hour exercise sessions including aerobic, resistance, respiratory, and balance/proprioceptive components. Sessions will be monitored and supervised by cardiologists, rehabilitation physicians, and physiotherapists. In addition, patients will attend one weekly in-person educational session throughout the 3-month program. |
Timeline
- Start date
- 2026-01-30
- Primary completion
- 2027-01-01
- Completion
- 2028-01-01
- First posted
- 2026-01-20
- Last updated
- 2026-01-20
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT07350941. Inclusion in this directory is not an endorsement.