PROM_R: Patient-Reported Outcome Measures in Cardiac Rehabilitation: Impact on Health Care

Sponsor
José Manuel Afonso Moreira (Other)
Overall Status
Recruiting
CT.gov ID
NCT06032013
Collaborator
(none)
25
1
1
15
1.7

Study Details

Study Description

Brief Summary

Cardiac Rehabilitation (CR) programs are a multidisciplinary process aimed at patient recovery after an acute cardiovascular event or with chronic heart disease, reducing mortality and morbidity, optimising functional capacity and improving quality of life. The aim is to maintain or recover the patient's clinical, physical and psychosocial condition, slowing down or halting the progression of the underlying disease process. It is based on the practice of personalized physical exercise and the adaptation of behaviours towards a healthier lifestyle, ensuring the reduction and control of risk factors. It is considered a cost-effective intervention that is explicitly and formally recommended by the most diverse and important scientific societies. Through the partnership and collaboration between the various health institutions and the academy, the CR program will take place on an outpatient basis, in a supervised manner, starting after risk stratification with a stress test and respective clinical assessment by a cardiologist. The coordinator of the CR program will be a cardiologist, and the entire multidisciplinary team will be responsible for effectiveness and safety, as well as patient assessment and progress.

Condition or Disease Intervention/Treatment Phase
  • Other: Cardiac rehabilitation program (PROMs)
N/A

Detailed Description

The outpatient CR program is designed for a group of participants who have had a cardiac event, based on the American College of Sports Medicine's Guidelines for Exercise Testing and Prescription, consisting of two exercise sessions/week. The sessions are supervised by a healthcare professional specialising in cardiac rehabilitation, and the participant's haemodynamic status is monitored continuously using scales and electronic equipment. PROMs will be applied before and after the program.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
25 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Patient-Reported Outcome Measures and Quality of Life in Cardiac Rehabilitation: Impact on Health Care
Actual Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cardiac Rehabilitation intervention

Outpatient intervention with participants after a cardiac event who fulfil the inclusion criteria.

Other: Cardiac rehabilitation program (PROMs)
The program is multidisciplinary with the following components: Medical assessment Physical training and counselling on physical activity Identification and control of risk factors Nutritional assessment and counselling Psychological assessment and intervention Education and information

Outcome Measures

Primary Outcome Measures

  1. EQ5D-5L: Health-related quality of life [Before the intervention and up to 8 weeks.]

    The EQ5D makes it possible to assess quality of life in a given pathology in the general population, presented in different domains. The visual analogue scale of this questionnaire has a score of 0-100. Higher scores mean a better result.

  2. HADS: Anxiety and depression [Before the intervention and up to 8 weeks.]

    Participants' anxiety and worries are also assessed. Mood disorders, weakness, worry, stress, and depression are common psychological repercussions for patients after a cardiac event, which can trigger hyperventilation reactions. This type of common reaction to emotional extremes such as fear, anxiety, or stress in participants can have a direct impact on involvement in CR programs. This questionnaire is made up of 14 questions. Lower scores mean a better result.

Secondary Outcome Measures

  1. Heart rate [Before, during and up to 8 weeks of the program.]

    Heart rate (bpm)

  2. Blood pressure [Before, during and up to 8 weeks of the program.]

    Blood pressure (mmHg)

  3. Peripheral oxygen saturation [Before, during and up to 8 weeks of the program.]

    Peripheral oxygen saturation (%)

  4. Exercise Capacity [During and up to 8 weeks of the program.]

    Borg scale- score 0-10. Higher values mean greater respiratory effort.

  5. Weight [Before the intervention and up to 8 weeks.]

    Weight (Kg)

  6. Abdominal perimeter [Before the intervention and up to 8 weeks.]

    Abdominal perimeter (cm)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult (> 18 years);

  • Low-moderate risk for physical exercise;

  • After a cardiac event;

  • Have signed an informed consent form.

Exclusion Criteria:
  • Physical or mental limitation to carry out an exercise programme;

  • Uncontrolled arrhythmia;

  • Severe chronic obstructive pulmonary disease;

  • Uncontrolled hypertension;

  • Symptomatic peripheral arterial disease;

  • Unstable angina;

  • Uncontrolled diabetes;

  • Acute pulmonary oedema in the last 12 hours;

  • Those who refuse to participate.

Contacts and Locations

Locations

Site City State Country Postal Code
1 National School of Public Health Lisbon Portugal

Sponsors and Collaborators

  • José Manuel Afonso Moreira

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
José Manuel Afonso Moreira, Principal Investigator, University of Évora
ClinicalTrials.gov Identifier:
NCT06032013
Other Study ID Numbers:
  • National School Public Health
First Posted:
Sep 11, 2023
Last Update Posted:
Sep 13, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Sep 13, 2023