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Nurse-Led Telehealth Frailty Management in Older Adults

The Effect of a Nurse-Led Telehealth-Supported Multicomponent Frailty Management Program on Frailty and Functional Status in Older Adults Living at Home: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07634406
Enrollment
100
Registered
2026-06-08
Start date
2026-06-05
Completion date
2026-10-15
Last updated
2026-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Frailty

Keywords

Older adults, Telehealth, Nursing intervention, Frailty management, Functional status, Home care

Brief summary

Frailty is an important geriatric syndrome associated with reduced physiological reserve, functional decline, falls, hospitalization, and increased health care use among older adults. This randomized controlled trial aims to evaluate the effect of a nurse-led telehealth-supported multicomponent frailty management program on frailty level and functional status in older adults living at home. The study will be conducted as a single-center, two-arm, parallel-group randomized controlled trial. A total of 100 older adults aged 65 years and older who are living at home and are frail or at risk of frailty will be randomly assigned to either the intervention group or the control group in a 1:1 ratio. Participants in the intervention group will receive an 6-week nurse-led telehealth-supported frailty management program, including weekly telephone counseling and individualized follow-up. Participants in the control group will continue usual care. Data will be collected at baseline, at 6 weeks, and at 18 weeks. The primary outcome is frailty level measured using the FRAIL Scale. Secondary outcomes include functional status, depressive symptoms, number of falls, emergency department visits, and hospitalizations.

Detailed description

The intervention includes frailty awareness, physical activity and mobility support, nutrition and fluid intake counseling, fall prevention and home safety, sleep and fatigue management, self-management, and healthy lifestyle behaviors. The program will be delivered by a nurse through an initial face-to-face assessment and weekly telephone counseling sessions lasting approximately 20 to 25 minutes over 6 weeks. Intervention fidelity will be monitored using a standardized checklist.

Interventions

BEHAVIORALNurse-Led Telehealth-Supported Multicomponent Frailty Management Program

The intervention is a structured 6-week multicomponent program delivered by a nurse. Following baseline assessment and individualized goal setting, participants will receive weekly telephone counseling sessions lasting approximately 20 to 25 minutes. The intervention covers frailty awareness, physical activity and mobility support, nutrition and fluid intake counseling, fall prevention and home safety, sleep and fatigue management, self-management, and healthy lifestyle behaviors. Intervention fidelity will be monitored using a standardized checklist.

Sponsors

Kutahya Health Sciences University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Participants will be randomized in a 1:1 ratio to either the nurse-led telehealth-supported frailty management program group or the usual care group.

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 65 years or older * Living at home and not receiving institutional care * Frail or at risk of frailty * Having sufficient hearing and cognitive ability to communicate by telephone * Able to read, understand, and communicate in Turkish * Providing written informed consent

Exclusion criteria

* Having advanced cognitive impairment such as dementia * Having hearing or speech problems that prevent communication * Being bedridden * Being in the terminal stage of illness * Participating in another intervention or education program at the same time * Having a serious physical or psychiatric condition that may prevent regular participation in the intervention

Design outcomes

Primary

MeasureTime frameDescription
Frailty Level Assessed by the FRAIL ScaleBaseline, 6 weeks, and 18 weeksFrailty level will be assessed using the FRAIL Scale. The FRAIL Scale consists of five components: fatigue, resistance, ambulation, illnesses, and weight loss. Total scores range from 0 to 5. Higher scores indicate greater frailty. A score of 0 indicates robust status, scores of 1 to 2 indicate pre-frailty, and scores of 3 to 5 indicate frailty.

Secondary

MeasureTime frameDescription
Functional Status Assessed by the Lawton-Brody Instrumental Activities of Daily Living ScaleBaseline, 6 weeks, and 18 weeksFunctional status will be assessed using the Lawton-Brody Instrumental Activities of Daily Living Scale. Total scores range from 0 to 8. Higher scores indicate greater independence in instrumental activities of daily living.
Depressive Symptoms Assessed by the 15-Item Geriatric Depression ScaleBaseline, 6 weeks, and 18 weeksDepressive symptoms will be assessed using the 15-item Geriatric Depression Scale. Total scores range from 0 to 15. Higher scores indicate more severe depressive symptoms. Scores of 0 to 4 indicate no depression, 5 to 8 indicate mild depression, 9 to 11 indicate moderate depression, and 12 to 15 indicate severe depression.
Number of Falls During the Study PeriodFrom baseline to 18 weeksThe number of falls experienced by participants during the study period will be recorded using a fall and health care utilization form developed by the researchers. Data will be based on participant self-report. A higher number indicates more falls.
Number of Emergency Department Visits During the Study PeriodFrom baseline to 18 weeksThe number of emergency department visits during the study period will be recorded using a health care utilization form developed by the researchers. Data will be based on participant self-report. A higher number indicates greater emergency health care utilization.
Number of Hospitalizations During the Study PeriodFrom baseline to 18 weeksThe number of hospitalizations during the study period will be recorded using a health care utilization form developed by the researchers. Data will be based on participant self-report. A higher number indicates greater hospital utilization.

Countries

Turkey (Türkiye)

Contacts

CONTACTSerkan Budak, PhD / RN
serkan.budak@ksbu.edu.tr+905385430616

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 28, 2026