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The Effect of NICE Support Program on Frailty and Quality of Life in Patients With Heart Failure

The Effect of NICE Support Program on Frailty and Quality of Life in Patients With Heart Failure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05366686
Acronym
NICE
Enrollment
240
Registered
2022-05-09
Start date
2022-01-18
Completion date
2024-02-08
Last updated
2025-07-10

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

Conditions

Frailty, Quality of Life

Keywords

Frailty, Quality of Life, Heart failure, Exercise program, nutrition

Brief summary

This RCT study aims to examine effects of a NICE Support Program in heart failure patients. The following hypotheses were tested: patients who received the NICE program will report significant improvement in frailty , social support, anxiety, and depression, quality of life, and nutritional assessment at baseline,4 weeks, 12 weeks and 24 weeks.

Detailed description

This study aims to develop NICE Support program, and examine the effects of an NICE program in heart failure patients. An experimental design is used. Subjects are selected using a purposeful sampling and are randomly assigned to the intervention or control group by using block size randomization method. Patients in the intervention group will receive a 12 week NICE Support program including: individual consultation, nutritional consultation, teaching exercise which contain walking and resistance exercise by using elastic bands and elastic balls. Data are collected by physical indicators and a structural questionnaire to measure frailty, quality of life, social support, anxiety and depression, symptom distress at baseline, 4 weeks, 12 weeks and 24 weeks . Data analysis includes descriptive statistics, Pearson correlation coefficient, independent t test, chi square, one way ANOVA and generalized estimating equation.

Interventions

BEHAVIORALNICE Support Program

Patients in experimental group will receive a 12 week NICE Support program; patients in control group maintain their usual life activities.

Sponsors

Ai-Fu Chiou
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Masking description

One research assistant is trained for being a outcomes assessor in this study who did not know the allocation of participants.

Intervention model description

Patients in the intervention group will receive a 12 week exercise program including: individual consultation, nutrition consultation, teaching exercise which contain walking and resistance exercise by using elastic bands and elastic balls.

Eligibility

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

Inclusion criteria

1. Aged above 20 and stable condition and had received physical activity. 2. Clear consciousness, can communicate with Chinese and Taiwanese. 3. Consent to join in this study. 4. Have a smartphone and be able to join social media(Line: heart together-go go go )

Exclusion criteria

1. Bed-ridden or unable to perform activities of daily living independently. 2. Unstable illness condition. 3. Emergency condition. 4. Contraindications of performing exercise such as uncontrolled hypertension, uncontrolled arrhythmia. 5. Patients with increased nerve, muscle, bone or rheumatoid diseases due to exercise

Design outcomes

Primary

MeasureTime frameDescription
Change Frailty Assessment Scale for Heart Failure, FAS-HF) and Clinical Frailty Scale scoresbaseline, 4week, 12 week, 24weekChanges from baseline Frailty Assessment Scale for Heart Failure, FAS-HF) scores including three indicators: physical, Psychological and social , at 6 weeks, 12 weeks, 24 weeks. FAS-HF scale contains 15 items, each item use Likert scale five point scoring, the total scores ranged from 0 to 45, the higher scores indicate higher frailty. Changes from baseline Clinical Frailty Scale including nine indicators, the higher scores indicate higher frailty.
Changes in symptoms distress scoresbaseline, 4week, 12 week, 24weekChanges from baseline symptoms distress scale at 4 weeks, 12 weeks, 24 weeks. Symptoms distress scale contains 17 common symptoms items, each item use Likert scale five point scoring, the total scores ranged from 17 to 85, the higher scores indicate worse symptom distress.

Secondary

MeasureTime frameDescription
The Minnesota living with heart failure questionnaire(MLHFQ)baseline, 4week, 12 week, 24weekChanges from baseline Minnesota living with heart failure questionnaire at 4 weeks, 12 weeks, 24 weeks. The Minnesota living with heart failure questionnaire contains 21 questions regarding the effects of heart failure on patients' physical (eight questions),emotional (five questions) and general (eight questions) dimensions. The possible answer for each question ranges from 0(no) to 5(a lot), and the total score range is 0-105; a higher score indicates lower quality of life .
Changes in anxiety and depression scoresbaseline, 4week, 12 week, 24weekChanges from baseline hospital anxiety and depression scale at 6 weeks, 12 weeks, 24 weeks. The hospital anxiety and depression scale contains 14 questions(7 for assess anxiety and 7 for assess depression), each item use Likert scale four point scoring, the total scores ranged from 0 to 21, the higher scores indicate more severe anxiety and depression level.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026