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Effects of a Food Supplement on Quality of Life in Patients With Chronic Obstructive Pulmonary Disease. (EPOCAT)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Food supplement
Placebo
Sponsored by
Arafarma Group, S.A.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Obstructive Pulmonary Disease

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults: men and women ≥ 18 years.
  • Patients with a medical diagnosis of COPD based on a recent spirometry.
  • Patients with a CAT score> 15, affecting COPD symptoms in a moderate-high way in the daily life of these patients.
  • Minimum clinical stability period of 4 weeks before the start of the study.
  • Patients who are trained to give informed consent.
  • Patients must agree to perform study visits and procedures with precise instructions.

Exclusion Criteria:

  • BMI ≥ 40.
  • Comorbidities, which due to their severity or progression, may interfere with the results, such as cancer, hematological disorders, severe heart or liver failure, kidney failure on dialysis, tuberculosis (TB) or AIDS, or other pulmonary pathologies such as pulmonary thromboembolism ( PE), pulmonary fibrosis, or relevant bronchiectasis.
  • In Pulmonary Rehabilitation treatment or in treatment for smoking.
  • Pregnancy or breastfeeding.
  • Impossibility of the patient, due to a medical condition, to follow the study.

Sites / Locations

  • Hospital Universitario Doctor Peset

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Food supplement

Placebo

Arm Description

One tablet a day, during 12 months

One tablet a day, during 12 months

Outcomes

Primary Outcome Measures

Change in quality of life
To assess the magnitude of the change from baseline quality of life at 3 months, 6 months, 9 months and 12 months using the COPD Assessment Test (CAT) scale in COPD patients with a CAT score> 15 who receive ARACOMPLEX® supplementation compared to those patients receiving placebo.

Secondary Outcome Measures

Full Information

First Posted
January 28, 2021
Last Updated
November 14, 2022
Sponsor
Arafarma Group, S.A.
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1. Study Identification

Unique Protocol Identification Number
NCT04815499
Brief Title
Effects of a Food Supplement on Quality of Life in Patients With Chronic Obstructive Pulmonary Disease.
Acronym
EPOCAT
Official Title
Study of the Impact on Quality of Life With ARACOMPLEX® Food Supplement Versus Placebo in Chronic Obstructive Pulmonary Disease Patients With a CAT Score> 15.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2022
Overall Recruitment Status
Completed
Study Start Date
January 14, 2020 (Actual)
Primary Completion Date
September 15, 2022 (Actual)
Study Completion Date
November 3, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Arafarma Group, S.A.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
It has been demonstrated that consequences of malnutrition affect a situation of risk and have negative effects on the evolution of chronic obstructive pulmonary disease (COPD), accompanied by higher morbidity and mortality. The impact of malnutrition on the respiratory system affects the respiratory muscles, the lung parenchyma, and the immune system. In summary, the risk of complications can lead to a worsening of the quality of life of the COPD patient. Also, dyspnea as the main symptom of COPD is the one that produces the greatest loss of quality of life, especially in older patients. The components of our authorized food supplement improve the quality of life of the patient. These components maintain the strength and energy of the patient, help the body to recover and regain its optimal state, help improve the immune system, help reduce the side effects of therapies associated with the control or cure of cancer and help correct nutritional deficiencies. This is the reason why this experimental study aims to improve the quality of life in patients with COPD with a CAT score>15.
Detailed Description
This study is developed in two phases: pilot phase and experimental phase. The pilot phase is preliminary and progressive in order to demonstrate a sufficient effect of improving the quality of life of patients and to be able to continue in an experimental phase with more investigational sites and more patients, and to evaluate other secondary objectives. Once the pilot phase is finished, an intermediate analysis of the results will be carried out to evaluate the magnitude of the variation in quality of life at 3, 6, 9 and 12 months. If the expected success expectations are achieved and it is approved by the Ethics Committee, the study will continue to the experimental phase.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
18 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Food supplement
Arm Type
Experimental
Arm Description
One tablet a day, during 12 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
One tablet a day, during 12 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Food supplement
Intervention Description
ARACOMPLEX® is an authorized food supplement that contains maca extract, vitamin complexes and ions, and that improves the quality of life of the patient.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo has a composition that makes its weight and organoleptic characteristics are identical to ARACOMPLEX®.
Primary Outcome Measure Information:
Title
Change in quality of life
Description
To assess the magnitude of the change from baseline quality of life at 3 months, 6 months, 9 months and 12 months using the COPD Assessment Test (CAT) scale in COPD patients with a CAT score> 15 who receive ARACOMPLEX® supplementation compared to those patients receiving placebo.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults: men and women ≥ 18 years. Patients with a medical diagnosis of COPD based on a recent spirometry. Patients with a CAT score> 15, affecting COPD symptoms in a moderate-high way in the daily life of these patients. Minimum clinical stability period of 4 weeks before the start of the study. Patients who are trained to give informed consent. Patients must agree to perform study visits and procedures with precise instructions. Exclusion Criteria: BMI ≥ 40. Comorbidities, which due to their severity or progression, may interfere with the results, such as cancer, hematological disorders, severe heart or liver failure, kidney failure on dialysis, tuberculosis (TB) or AIDS, or other pulmonary pathologies such as pulmonary thromboembolism ( PE), pulmonary fibrosis, or relevant bronchiectasis. In Pulmonary Rehabilitation treatment or in treatment for smoking. Pregnancy or breastfeeding. Impossibility of the patient, due to a medical condition, to follow the study.
Facility Information:
Facility Name
Hospital Universitario Doctor Peset
City
Valencia
ZIP/Postal Code
46017
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Effects of a Food Supplement on Quality of Life in Patients With Chronic Obstructive Pulmonary Disease.

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