Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT07435064

NURsing-led FRAILty Prevention and Care

The goal of this quasi-experimental study is to learn if a nurse-led care program can help prevent or manage frailty in older adults living in the community.

The study focuses on people aged 65 years and older who have at least one chronic condition, show early signs of frailty, and have difficulty with self-care.

The main questions it aims to answer are:

* Does the nurse-led NUR-FRAIL program improve participants' ability to care for their chronic conditions after six months? * Does the program improve quality of life and reduce health-related difficulties? * Does the program lower emergency department visits and hospital stays over one year?

Researchers will compare participants who receive the NUR-FRAIL program with participants who receive usual care to see if the program leads to better self-care, better quality of life, and less use of hospital services.

Participants will:

* Meet with a Family and Community Nurse for health and frailty assessments at the start of the study, after three months, and after six months * Complete short questionnaires about self-care, daily functioning, and quality of life * Receive either usual care or a three-month nurse-led program that includes personalized education, goal setting, lifestyle advice, and support for managing chronic conditions * Allow researchers to collect information about emergency visits and hospital stays for up to twelve months

Some participants in the nurse-led group will also be invited to take part in an interview to share their experience with the program.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

NUR-FRAIL (NURsing-led FRAILty Prevention and Care) is a multicenter quasi-experimental controlled study designed to evaluate the effectiveness of a structured nurse-led intervention for the prevention and management of frailty in community-dwelling older adults. Study Design and Setting This is a 12-month multicenter quasi-experimental study conducted within Family and Community Nursing Services in four districts of ULSS 7 Pedemontana (Italy). Allocation to intervention or control group is determined at the service level based on organizational feasibility to ensure comparable care contexts.

All participants undergo standardized assessments at baseline, three months, and six months. Healthcare utilization data are collected at six and twelve months.

Intervention Participants in the intervention group receive the NUR-FRAIL program over three months, delivered by trained Family and Community Nurses through in-person (clinic or home) and/or telephone contacts. The intervention includes at least four structured contacts.

The program integrates the WHO ICOPE framework and consists of:

Structured multidimensional assessment of frailty, including evaluation of cognitive function, mobility, nutritional status, vision, hearing, depressive symptoms, social support, caregiver burden, and urinary incontinence.

Identification of participant-prioritized needs, using open-ended assessment to capture individual concerns and goals.

Individualized therapeutic education pathway, including:

Functional ability enhancement Chronic disease self-care support Lifestyle modification (physical activity, nutrition, hydration, sleep, fall prevention, vaccination, medication adherence, cardiovascular risk management, cognitive stimulation, social participation) SMART goal setting (Specific, Measurable, Achievable, Realistic, Time-bound).

Evidence-based communication strategies, including:

Teach-back method Motivational interviewing Shared decision-making using the SHERPA model Family-centered approaches when appropriate Participants receive tailored educational materials developed in alignment with ICOPE recommendations.

Nurses delivering the intervention receive structured training sessions to ensure fidelity to the model.

Participants in the control group receive usual care provided by the Family and Community Nursing Services.

Outcomes The primary outcome is self-care maintenance at six months, measured using the Self-Care of Chronic Illness Inventory.

Secondary outcomes include:

Self-care monitoring and self-care management Self-reported health complexity Health-related quality of life Emergency department visits Hospitalizations related to chronic conditions or frailty

Data Collection and Analysis Quantitative data include socio-demographic and clinical variables, questionnaire scores, and healthcare utilization records. Statistical analyses will include descriptive statistics, between-group comparisons, and regression models to adjust for potential confounders. Statistical significance will be set at p < 0.05.

Qualitative data will be collected through semi-structured interviews with a purposive subsample of participants in the intervention group. Interviews will explore satisfaction, perceived benefits, and areas for improvement. Transcripts will undergo content analysis performed independently by trained researchers to ensure methodological rigor.

Sample Size and Ethics The study is powered to detect a clinically meaningful difference in self-care maintenance between groups. Accounting for expected attrition, approximately 200 participants will be enrolled. All participants will provide written informed consent. Data will be managed in compliance with European data protection regulations (GDPR).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Presence of at least one positive indicator on the SUNFRAIL questionnaire
  • Age 65 years or older
  • At least one chronic condition
  • Poor self-care abilities, defined as a score of 0, 1, or 2 on at least two items of the Self-Care of Chronic Illness Inventory

Exclusion criteria

  • Not able to provide information on questionnaires

Treatment and study plan

NUR-FRAIL

Behavioral

Participants in this arm receive the NUR-FRAIL nurse-led program in addition to usual care.

The program is delivered by Family and Community Nurses over a three-month period and includes at least four structured contacts (clinic visits, home visits, and/or telephone contacts).

The intervention starts with a comprehensive frailty assessment based on the World Health Organization Integrated Care for Older People (ICOPE) framework, followed by personalized education and shared goal setting.

Key components include:

Multidimensional frailty assessment (mobility, nutrition, cognition, mood, vision, hearing, social support, caregiver burden, and urinary continence)

Identification of participant priorities and care needs

Individualized education to support self-care and functional ability

Lifestyle guidance (physical activity, nutrition, hydration, fall prevention, medication adherence, sleep, mental well-being, and social participation)

Shared SMART goal setting

Use of evidence-based

Primary outcomes

  1. Self-care maintenance was assessed using the Self-Care of Chronic Illness Inventory questionnaire (minimum score = 0, maximum score = 100), where higher scores indicate better self-care.

    Time frame: SIX MONTHS

    Self-care maintenance was assessed using the Self-Care of Chronic Illness Inventory (minimum score = 0, maximum score = 100), where higher scores indicate better self-care.

Secondary outcomes

  1. Self-care monitoring was assessed using the Self-Care of Chronic Illness Inventory questionnaire (minimum score = 0, maximum score = 100), where higher scores indicate better self-care.

    Time frame: three and six months

    Self-care monitoring was assessed using the Self-Care of Chronic Illness Inventory questionnaire (minimum score = 0, maximum score = 100), where higher scores indicate better self-care.

  2. Self-care management was assessed using the Self-Care of Chronic Illness Inventory questionnaire (minimum score = 0, maximum score = 100), where higher scores indicate better self-care.

    Time frame: three and six months

    Self-care management was assessed using the Self-Care of Chronic Illness Inventory questionnaire (minimum score = 0, maximum score = 100), where higher scores indicate better self-care.

  3. Self-perceived patient complexity was assessed using the INTERMED questionnaire (minimum score = 0, maximum score = 60), where higher scores indicate greater patient complexity.

    Time frame: three and six months

    Self-perceived patient complexity was assessed using the INTERMED questionnaire (minimum score = 0, maximum score = 60), where higher scores indicate greater patient complexity.

  4. Quality of life was assessed using the 12-Item Short Form Health Survey (SF-12) (minimum score = 0, maximum score = 100), where higher scores indicate better quality of life.

    Time frame: three and six months

    Quality of life was assessed using the 12-Item Short Form Health Survey (SF-12) (minimum score = 0, maximum score = 100), where higher scores indicate better quality of life.

  5. Number of emergency department access by patient

    Time frame: six and 12 months

    Number of emergency department access by patient

  6. Number of hospitalization by patient

    Time frame: six and 12 months

    Number of hospitalization by patient

Study contacts

Contact information is provided by the study sponsor or research team.

Jessica Longhini

CONTACT

[email protected]

3405322936

Sponsors and collaborators

Lead sponsor

University of Padova

Other

Registry information

Official study title

NURsing-led FRAILty Prevention and Care: a Quasi-experimental Study

Acronym: NUR-FRAIL

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Feb 27, 2026
Registry last updated
Feb 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.