A Service-Learning Program for Comprehensive Geriatric Assessment and Health Promotion in Older Adults (GEROS)

March 19, 2025 updated by: Javier Jerez Roig, University of Vic - Central University of Catalonia

The GEROS Project aims to develop and implement a Service-Learning (S-L) program that integrates Comprehensive Geriatric Assessment (CGA) and health promotion, for students at the Faculty of Health Sciences and Welfare at the University of Vic - Central University of Catalonia (UVic-UCC). This initiative engages university students, healthcare professionals, and older adults (60+) in a participatory, intergenerational approach that fosters mutual learning and community engagement.

The study follows a non-experimental mixed-method design, involving students from Nursing, Physiotherapy, Human Nutrition and Dietetics, Occupational Therapy, and Psychology. Participants include older adults (60+) who can independently travel to the university.

The project is integrated into different subjects, in groups of 4-5 students, participants conduct a Comprehensive Geriatric Assessment (CGA), evaluating frailty using VIG-Frail, intrinsic capacity with ICOPE, quality of life with EUROQOL 5D-5L, and specific health indicators with Nursing Outcomes Classification (NOC).

To assess the program's effectiveness, several outcome measures will be analyzed including students' perceived knowledge, competencies, and skills, as well as older adults' awareness of their health status, lifestyle, and risk factors. Additionally, the satisfaction levels of both will be evaluated. The items will be evaluated using a 1-5 Likert Scale, and the analysis will be conducted with SPSS. Data recording will be carried out through REDCap.

The GEROS Project aligns with the United Nations' Sustainable Development Goals (SDGs), specifically SDG 3 (Good Health and Well-being) and SDG 10 (Reduced Inequalities). By offering care to the aging population and providing them with personalized health recommendations, the project promotes preventive strategies, active aging, and intergenerational learning.

Furthermore, GEROS integrates innovative educational methodologies, encouraging experiential learning, collaboration with healthcare professionals, and the development of practical skills in real-world contexts. The program's scalability and adaptability could serve as a model for other universities and healthcare institutions aiming to enhance geriatric care through service-learning initiatives.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Barcelona
      • Vic, Barcelona, Spain, 08500
        • Recruiting
        • Faculty of Health Sciences and Welfare
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

A) For users:

  • Any person aged 60 or older who can move to the facility (Faculty of Health Sciences and Welfare) independently or accompanied by a caregiver.

B) For students:

  • Students from Nursing, Physiotherapy, Nutrition and Dietetics, Occupational Therapy and Psychology degrees of UVic-UCC.

Exclusion Criteria:

  • For users: Individuals institutionalized in a long-term care institution.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Screening
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Comprehensive geriatric assessment.
The intervention will consist of a total of 3 sessions which will take place in different areas of the Faculty of Health and Welfare Sciences (FCSB) at the University of Vic - Central University of Catalonia. In Session 1, a comprehensive geriatric assessment (CGA) will be conducted to the users (by students supervised by health professionals).
A report with the results of the CGA and health recommendations will be delivered to the users. They will receive health education including specific recommendations and community health resources based on their health status and CGGA.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Frailty
Time Frame: Baseline assessment
VIG-Frail is a screening tool used to assess frailty in older adults. It's a short, easy-to-administer test that helps healthcare providers identify individuals who may be at risk of adverse health outcomes due to frailty.
Baseline assessment
Users Satisfaction with treatment
Time Frame: Up to 2-4 weeks (Post-intervention - 2nd session)
Evaluation of the user's general satisfaction with participating in the project (5-point Likert scale from 1-not at all to 5-very satisfied)
Up to 2-4 weeks (Post-intervention - 2nd session)
Students Satisfaction with intervention
Time Frame: At the end of Session 1 (CGA of users)
Evaluation of the students' general satisfaction with the participation in the study (5-point Likert scale from 1-not at all to 5-very satisfied)
At the end of Session 1 (CGA of users)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-reported Quality of Life
Time Frame: Baseline assessment
Quality of Life measured with EuroQol 5D-5L, a standardised tool used to measure and assess health-related quality of life. The "5D" refers to five dimensions of health: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension has five levels, ranging from "no problems" to "extreme problems," allowing for a detailed assessment of a person's health status.Health state index scores generally range from less than 0 (where 0 is the value of a health state equivalent to dead; negative values representing values as.
Baseline assessment
Intrinsic capacity
Time Frame: Baseline assessment

Integrated care for older people approach (ICOPE) is a framework developed by the World Health Organization to support the health and well-being of older adults through comprehensive, integrated care.

It focuses on 7 key dimensions: cognitive decline, limited mobility, undernutrition, vision impairment, hearing loss, depressive symptoms, and social care and supports, as well as carer support and urinary incontinence. These areas are assessed to create a holistic care plan tailored to the individual's needs. This outcome will be categorized according to the number or preserved dimensions: from 7 (all 7 dimesions preserved) to 0 (all 7 dimensions affected).

Baseline assessment
Nursing Outcomes Classification
Time Frame: Baseline assessment

The NOC (Nursing Outcomes Classification) is a system used to assess the results of nursing care, helping to measure a person's level of functioning and well-being in different areas of health.

The NOC outcomes evaluated in this context are: Cognition, Mobility, Nutritional Status, Sensory Function: Vision, Desire to Live, Caregiver Well-being Urinary Continence, Psychosocial Adjustment: Life Change These outcomes are assessed using a 5-point Likert scale, ranging from 1 (Not demonstrated) to 5 (Always demonstrated).

Baseline assessment
Students Self-perception of increased knowledge, skills and competencies
Time Frame: At the end of Session 1 (CGA of users)
Knowledge about Health Promotion and Disease Prevention, Improvement in Skills and Technical Competencies in Comprehensive Geriatric Assessment (CGA), Skills and Technical Competencies in Intrinsic Capacity (ICOPE), Transversal Skill "Communication", Critical Thinking, Integration of Knowledge, Skills, and Competencies in the subject in Which the project Was Held, Problem-Solving Ability, Interdisciplinary. These outcomes are assessed using a 5-point Likert scale, ranging from 1 (Not demonstrated) to 5 (Always demonstrated).
At the end of Session 1 (CGA of users)
Users Self-perception of increased knowledge, skills and competencies
Time Frame: Up to 2-4 weeks (Post-intervention - 2nd session)
Knowledge about Their Own Health, Lifestyle and Risk Factors to Modify for increasing Health and Disease Prevention and Community Health Resources, evaluated with a Likert scale from 1 to 5 (1 = not much, 5 = very much)
Up to 2-4 weeks (Post-intervention - 2nd session)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Júlia Casacuberta-Roca, Nursing, University of Vic - Central University of Catalonia

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 11, 2024

Primary Completion (Estimated)

December 20, 2025

Study Completion (Estimated)

December 20, 2025

Study Registration Dates

First Submitted

March 5, 2025

First Submitted That Met QC Criteria

March 19, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 19, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 24/082
  • 2023 IMPAC 00014 (Other Grant/Funding Number: AGAUR)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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