Nutritional Support and Telemedicine

Sponsor
Consorci Sanitari Integral (Other)
Overall Status
Recruiting
CT.gov ID
NCT05815914
Collaborator
(none)
182
1
2
25
7.3

Study Details

Study Description

Brief Summary

The aim of this clinical trial is to assess the implementation of an APP to track the nutritional status and diet habits of "chronic complex patients"(CCP) in order to improve their nutritional status and evaluate the level of adherence to dietetic counseling.

Condition or Disease Intervention/Treatment Phase
  • Other: app
  • Other: control group
N/A

Detailed Description

The aim is to evaluate the usage of an APP and track the nutritional status of "chronic complex patients"(CCP) in order to improve their nutritional status.

This is a study of an experimental design, referring to a controlled randomized trial with CCP in the Moises Broggi hospital.In the first stage, there's been an elaboration of the contents of the APP. For the assessment of the strategy of food education, two groups of patients will be defined(Intervention group (IG) & Control group (CG)). In each group there will be 91 subjects, meaning a total of 182 patients. Inclusion criteria: >18 years old, CCP with either malnutrition, or risk of malnutrition (MNA<23,5), therapeutic profile <3, living at home, with full accessibility and capable to use a smartphone, and usual internet consumers (patients or caregivers), and who need to sign the informative consent. The inclusion of this study, will be made through a random sampling and patients will be assigned to IG or CG. All patients will undergo an initial evaluation, a follow-up visit after the first 6 months, and then a final visit after 12 months. The intervention group will also contain an educational, and nutritional program by means of the APP throughout the entire study, and data will be collected through a telematic questionnaire between visits. The variables to study are nutritional, diet, clinics, social and valorisation tools ICT (IG).

Study Design

Study Type:
Interventional
Anticipated Enrollment :
182 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Diagnostic
Official Title:
Dietetic Education Support, and Nutrition to Chronic Complex Patients With the Usage of a Telemedicine Tool
Actual Study Start Date :
Apr 1, 2022
Anticipated Primary Completion Date :
Apr 30, 2023
Anticipated Study Completion Date :
Apr 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention group

Other: app
The app will include a nutritional education programme through the APP throughout the study. At 2, 4, 6 and 8 months data will be collected through a telematics questionnaire

Active Comparator: Control group

Other: control group
Routine nutritional and dietary recommendations will be given.

Outcome Measures

Primary Outcome Measures

  1. Changes in nutritional status [Baseline and 12 months]

    Assessment of changes in nutritional status through the Mini Nutrition Assessment (MNA) at baseline and at 12 months

Secondary Outcome Measures

  1. Adherence to the Mediterranean diet [12 months]

    Assessment of adherence to the Mediterranean diet will be carried out with by Predimed questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 years old

  • polymorbidity

  • malnourished patient or patient at risk of malnutrition (MNA≤23.5)

  • patient living at home, with access to and able to use a smartphone and regular internet users (patients or caregivers)

  • patient who agrees to participate in the study by signing the informed consent form

Exclusion Criteria:
  • established artificial nutrition

  • advanced dementia

  • admission to a nursing home/social care for a period of >1 month

  • patients not responding to the telematic visits on more than 2 occasions.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital de Sant Joan Despí, CSI Sant Joan Despí Barcelona Spain 08970

Sponsors and Collaborators

  • Consorci Sanitari Integral

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Consorci Sanitari Integral
ClinicalTrials.gov Identifier:
NCT05815914
Other Study ID Numbers:
  • 20/92
First Posted:
Apr 18, 2023
Last Update Posted:
Apr 18, 2023
Last Verified:
Apr 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Consorci Sanitari Integral
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 18, 2023