Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT07190066

MELIORA Data Collection Campaigns

Led by Harokopio University · Updated on 2025-09-30

300

Participants Needed

7

Research Sites

23 weeks

Total Duration

On this page

Sponsors

H

Harokopio University

Lead Sponsor

B

BROSTCANCERFORENINGEN AMAZONA I STOCKHOLMS LAN

Collaborating Sponsor

AI-Summary

What this Trial Is About

To support the development of the MELIORA digital app for the MELIORA main intervention, an initial pilot study (Data Collection Campaign, DCC) is being conducted with the three target participant groups: healthy women at increased risk of developing breast cancer (BC), BC patients, and BC survivors across the four intervention countries (Spain, Greece, Lithuania, Sweden). The planned sample size for each group is 156 healthy women at risk (defined as not meeting recommendations for a healthy lifestyle), 58 BC patients, and 86 BC survivors. Each participant is asked to test and evaluate a preliminary version of the MELIORA app over a 14-day period. The DCC takes place in the early stages of the project, as part of the intervention development phase, to inform the technical refinement and preliminary evaluation of the MELIORA digital app.

CONDITIONS

Official Title

MELIORA Data Collection Campaigns

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals residing in Greece, Lithuania, Spain or Sweden
  • Female adults aged 18 years or older
  • Ability to understand and complete outcome measures in a local language of the participating countries
  • Ability to provide fully informed consent
  • Access to and ability to use a smartphone that supports the MELIORA app (iOS or Android)
  • Healthy women with BMI ≥ 25 or not meeting WHO recommendations of ≥150 minutes of moderate-to-vigorous physical activity per week
  • Women currently undergoing active breast cancer treatment or awaiting active treatment
  • Breast cancer survivors who completed active treatment at least six months prior to enrollment
Not Eligible

You will not qualify if you...

  • Inability to provide fully informed consent
  • Inability to understand or communicate in one of the recruitment countries' local languages

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

Harokopio University

Athens, Greece

Actively Recruiting

2

Lietuvos Sveikatos Mokslų Universitetas (Lsmu)

Kaunas, Lithuania

Actively Recruiting

3

Pagalbos Onkologiniams Ligoniams Asociacija (Pola L T)

Kaunas, Lithuania

Actively Recruiting

4

Fundación Para El Fomento de La Investigación Sanitaria Y Biomédica de La Comunitat Valenciana (Fisabio)

Valencia, Spain

Actively Recruiting

5

INCLIVA - Instituto de Investigación Sanitaria

Valencia, Spain

Actively Recruiting

6

Bröstcancerföreningen Amazona I Stockholms Län (Amazona)

Stockholm, Sweden

Actively Recruiting

7

Karolinska Institutet

Stockholm, Sweden

Actively Recruiting

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Research Team

Y

Yannis Manios, Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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