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Tackling Disruptions to Frailty Interventions: Developing Personalized Interventions Targeted for Older Persons With Cardiac Frailty (INDEPENDENCY)

Primary Purpose

Cardiovascular Diseases

Status
Recruiting
Phase
Not Applicable
Locations
Singapore
Study Type
Interventional
Intervention
Intervention Set A
Intervention Set B
Intervention Set C
Sponsored by
National Heart Centre Singapore
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiovascular Diseases focused on measuring Frailty, Intervention, Cardiac Frailty Interventions

Eligibility Criteria

21 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age ≥ 21 years old Outdoor ambulant Exclusion Criteria: Bed-bound Dementia (Stage 6 onwards) Residing in sheltered or nursing home Cancer (to avoid confounding with cardiac disease sequelae from cancer) Participation in ongoing clinical trials that involve interventional drugs or devices Uncontrolled hypertension (systolic blood pressure ≥160mmHg and/or diastolic blood pressure ≥90mmHg) despite being on treatment for hypertension Low blood pressure (systolic blood pressure <90mmHg or diastolic blood pressure <40mmHg) Uncontrolled atrial fibrillation (controlled atrial fibrillation is allowed) Ventricular arrhythmias (such as ventricular tachycardia) Renal failure on dialysis Chronic kidney disease Stage 4 and above Nephrotic syndrome Liver cirrhosis Child's B and above Inflammatory Bowel Disease Severe uncontrolled gout Poorly controlled Diabetes Hba1c ≥9% On warfarin Presence of food allergies (such as shell-fish, prawn) Patient's life expectancy is expected to be less than one year at the time of potential enrolment as assessed by the investigator Nasogastric or parenteral nutrition Hypertrophic cardiomyopathy Cardiac amyloidosis Cardiac sarcoidosis

Sites / Locations

  • Alexandra HospitalRecruiting
  • National Heart Centre SingaporeRecruiting
  • Changi General HospitalRecruiting
  • Sengkang General HospitalRecruiting
  • Jurong Community HospitalRecruiting
  • NHG PolyclinicsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

No Intervention

Experimental

No Intervention

Experimental

No Intervention

Arm Label

Outpatient clinic/community participants receiving exercise sessions and meals (A1)

Outpatient clinic/community participants receiving control/usual care (A2)

Step-down community hospital participants receiving exercise sessions and meals (B1)

Step-down community hospital participants receiving control/usual care (B2)

Acute hospital participants receiving meals (C1)

Acute hospital participants receiving control/usual care (C2)

Arm Description

Outpatient clinic/community participants receiving intervention Set A (exercise sessions and meals over approximately 12 weeks)

Outpatient clinic/community participants receiving control/usual care

Step-down community hospital participants receiving Intervention Set B (exercise sessions and meals over approximately 3 weeks)

Step-down community hospital participants receiving control/usual care

Acute hospital participants receiving Intervention Set C (meals over approximately 3 weeks)

Acute hospital participants receiving control/usual care

Outcomes

Primary Outcome Measures

Improvement in cardiovascular markers
Change in cardiovascular variables are diastolic function variables such as mitral annular velocities (m/s) OR; Change in Aerobic capacity (V02, ml/kg/min)
Improvement in skeletal muscle
Change in skeletal muscle mass (grams)
Improvement in Fried Frailty Phenotype Score (improvement in any domain) (i.e., reduction in score)

Secondary Outcome Measures

Improvement in metabolite level
Any change in metabolite (microM)
Improvement in Quality of life (QOL): EuroQOL-5D-5L (higher score)
A unit increase (i.e., improvement) in QOL score

Full Information

First Posted
June 15, 2023
Last Updated
August 6, 2023
Sponsor
National Heart Centre Singapore
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1. Study Identification

Unique Protocol Identification Number
NCT05946174
Brief Title
Tackling Disruptions to Frailty Interventions: Developing Personalized Interventions Targeted for Older Persons With Cardiac Frailty
Acronym
INDEPENDENCY
Official Title
Tackling Disruptions to Frailty Interventions: Developing Personalized Interventions Targeted for Older Persons With Cardiac Frailty
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 12, 2023 (Actual)
Primary Completion Date
June 21, 2028 (Anticipated)
Study Completion Date
June 21, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Heart Centre Singapore

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Muscle mass loss and metabolic dysfunction, exacerbated by inactivity and nutritional inadequacies, underpin both cardiovascular disease and frailty in ageing. The investigators' proposal seeks to develop interventions in exercise and diet that are targeted for older adults with cardiac frailty. Methods: The investigators' proposal is a five-year study comprising of first phase (first 2-2.5 years) and second phase (next 2-2.5 years). In the first phase cardiac frail participants (up to N=500) from each healthcare transition (inpatient hospital, step-down community hospital, outpatient clinic/community) will be randomized to receive Intervention Sets or usual care. The second phase will scale up these programs. Three Intervention Sets A, B, and C will be implemented in the outpatient, step-down community hospital, and acute hospital settings. Diet intervention comprises meal sets prepared with nutrients involved in energy metabolism. Exercise training is facilitated by hospital gyms and hospital physiotherapists. Diet and exercise behavior will be monitored using questionnaires, video conferencing and meal photos. Significance: Clinical studies are urgently needed using consistent frailty tools to evaluate the efficacy and promise of frailty interventions, targeted to achieve reversal/retardation of frailty. When scaled up, these approaches will provide high-quality science needed to manage cardiac frailty towards healthier population ageing.
Detailed Description
BACKGROUND Cardiovascular disease is a formidable disruptor of interventions related to exercise intervention. Patients and physicians face uncertainty about dispensing safe and effective exercise programs to frail patients with concomitant cardiovascular disease. This hesitancy permeates across transitions from acute to step-down care to community settings. Uncertainties include fear of exacerbating heart conditions, individual variability in exercise response and what exercise targets to reach that is rational for each patient. Often, little or no exercise intervention is applied in the acute to step-down phases, which are the periods most critical for frailty reversal. Current dietary interventions do not address the special nutritional needs of acute cardiovascular conditions like heart failure, and may paradoxically induce a syndrome of cardiac cachexia that contributes to the downward spiral of frailty. STUDY DESIGN: This will be a prospective randomized clinical trial. The investigators' proposal is a five-year study comprising of first phase (first 2-2.5 years) and second phase (next 2-2.5 years). In the first phase cardiac frail participants (up to N=500) from each healthcare transition (inpatient hospital, step-down community hospital, outpatient clinic/community) will be randomized to receive Intervention Sets or usual care. The second phase will scale up these programs. At enrolment, pre-defined study time points and end of study, participants will undergo assessments of clinical status, frailty status, cardiovascular function, nutrition, quality of life (QOL), diet/exercise behaviour, and biospecimen sampling. Three Intervention Sets will be implemented in the outpatient, step-down community hospital, and acute hospital settings. Diet intervention comprises meal sets prepared with nutrients involved in energy metabolism. During the trial, exercise intervention is performed in hospitals and community hospitals by physiotherapists. Associated factors such as dietary, comorbidities and other related habits will be tracked simultaneously during the trial Intervention Set A: exercise sessions and meals over approximately 12 weeks. Intervention Set B : exercise sessions and meals over approximately 3 weeks. Intervention Set C: meals over approximately 3 weeks. PROCEDURES Baseline Procedures i. Cardiovascular measurements Non-invasive brachial blood pressure machine Echocardiography Electrocardiography ii. Biospecimen collection iii. Six-minute walk test iv. Musculoskeletal Analysis v. Cardiopulmonary exercise test (CPET)/ Treadmill vi. Questionnaires vii. Timed up and go (TUG) test Post-intervention procedures i. Cardiovascular measurements Non-invasive brachial blood pressure machine Echocardiography Electrocardiography ii. Biospecimen collection iii. Six-minute walk test iv. Musculoskeletal Analysis v. Questionnaires vi. Timed up and go (TUG) test Closing questionnaires

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases
Keywords
Frailty, Intervention, Cardiac Frailty Interventions

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Set A comprises of outpatient clinic/ community participants, who will be randomized in a 1:1 ratio into Group A1 (receiving Intervention Set A- exercise sessions and meals over approximately 12 weeks) or Group A2 (control/ usual care) Set B comprises of step-down community hospital participants, who will be randomized in a 1:1 ratio into Group B1 (receiving Intervention Set B- exercise sessions and meals over approximately 3 weeks) or Group B2 (control/ usual care) Set C comprises of acute community hospital participants, who will be randomized in a 1:1 ratio into Group C1 (receiving Intervention Set C- meals over approximately 3 weeks) or Group C2 (control/ usual care)
Masking
None (Open Label)
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Outpatient clinic/community participants receiving exercise sessions and meals (A1)
Arm Type
Experimental
Arm Description
Outpatient clinic/community participants receiving intervention Set A (exercise sessions and meals over approximately 12 weeks)
Arm Title
Outpatient clinic/community participants receiving control/usual care (A2)
Arm Type
No Intervention
Arm Description
Outpatient clinic/community participants receiving control/usual care
Arm Title
Step-down community hospital participants receiving exercise sessions and meals (B1)
Arm Type
Experimental
Arm Description
Step-down community hospital participants receiving Intervention Set B (exercise sessions and meals over approximately 3 weeks)
Arm Title
Step-down community hospital participants receiving control/usual care (B2)
Arm Type
No Intervention
Arm Description
Step-down community hospital participants receiving control/usual care
Arm Title
Acute hospital participants receiving meals (C1)
Arm Type
Experimental
Arm Description
Acute hospital participants receiving Intervention Set C (meals over approximately 3 weeks)
Arm Title
Acute hospital participants receiving control/usual care (C2)
Arm Type
No Intervention
Arm Description
Acute hospital participants receiving control/usual care
Intervention Type
Other
Intervention Name(s)
Intervention Set A
Intervention Description
exercise sessions and meals over approximately 12 weeks
Intervention Type
Other
Intervention Name(s)
Intervention Set B
Intervention Description
exercise sessions and meals over approximately 3 weeks
Intervention Type
Other
Intervention Name(s)
Intervention Set C
Intervention Description
meals over approximately 3 weeks
Primary Outcome Measure Information:
Title
Improvement in cardiovascular markers
Description
Change in cardiovascular variables are diastolic function variables such as mitral annular velocities (m/s) OR; Change in Aerobic capacity (V02, ml/kg/min)
Time Frame
at 14 weeks from baseline
Title
Improvement in skeletal muscle
Description
Change in skeletal muscle mass (grams)
Time Frame
at 14 weeks from baseline
Title
Improvement in Fried Frailty Phenotype Score (improvement in any domain) (i.e., reduction in score)
Time Frame
at six months from baseline
Secondary Outcome Measure Information:
Title
Improvement in metabolite level
Description
Any change in metabolite (microM)
Time Frame
Three months and six months from baseline
Title
Improvement in Quality of life (QOL): EuroQOL-5D-5L (higher score)
Description
A unit increase (i.e., improvement) in QOL score
Time Frame
Three months and six months from baseline
Other Pre-specified Outcome Measures:
Title
Proportion of participants who experience a major adverse cardiovascular events
Description
Include cardiac mortality, acute myocardial infarction, unstable angina, any revascularization, heart failure, atrial fibrillation, strokes
Time Frame
Thirty-six (36) months from baseline
Title
Other events include proportion of participants who experience : death, falls, fractures, hospitalization for any cause, admission into nursing home
Time Frame
Thirty-six (36) months from baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 21 years old Outdoor ambulant Exclusion Criteria: Bed-bound Dementia (Stage 6 onwards) Residing in sheltered or nursing home Cancer (to avoid confounding with cardiac disease sequelae from cancer) Participation in ongoing clinical trials that involve interventional drugs or devices Uncontrolled hypertension (systolic blood pressure ≥160mmHg and/or diastolic blood pressure ≥90mmHg) despite being on treatment for hypertension Low blood pressure (systolic blood pressure <90mmHg or diastolic blood pressure <40mmHg) Uncontrolled atrial fibrillation (controlled atrial fibrillation is allowed) Ventricular arrhythmias (such as ventricular tachycardia) Renal failure on dialysis Chronic kidney disease Stage 4 and above Nephrotic syndrome Liver cirrhosis Child's B and above Inflammatory Bowel Disease Severe uncontrolled gout Poorly controlled Diabetes Hba1c ≥9% On warfarin Presence of food allergies (such as shell-fish, prawn) Patient's life expectancy is expected to be less than one year at the time of potential enrolment as assessed by the investigator Nasogastric or parenteral nutrition Hypertrophic cardiomyopathy Cardiac amyloidosis Cardiac sarcoidosis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Angela Su-Mei Koh
Phone
+65 6704 8961
Email
angela.koh.s.m@singhealth.com.sg
First Name & Middle Initial & Last Name or Official Title & Degree
Gina Sihui Lee
Phone
+65 6704 2228
Email
gina.lee.s.h@nhcs.com.sg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Angela Su-Mei Koh, MBBS, MPH
Organizational Affiliation
National Heart Centre Singapore
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alexandra Hospital
City
Singapore
ZIP/Postal Code
159964
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laureen Yi-Ting Wang
Facility Name
National Heart Centre Singapore
City
Singapore
ZIP/Postal Code
169609
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Angela Su-Mei Koh, MBBS, MPH
Phone
+65 6704 8961
Email
angela.koh.s.m@singhealth.com.sg
First Name & Middle Initial & Last Name & Degree
Gina Sihui Lee
Phone
+65 6704 2228
Email
gina.lee.s.h@nhcs.com.sg
Facility Name
Changi General Hospital
City
Singapore
ZIP/Postal Code
529889
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chun How Ooi
Facility Name
Sengkang General Hospital
City
Singapore
ZIP/Postal Code
544886
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zijuan Huang
Facility Name
Jurong Community Hospital
City
Singapore
ZIP/Postal Code
609606
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alvin Ong
Facility Name
NHG Polyclinics
City
Singapore
Country
Singapore
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shu Yun Tan

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29802321
Citation
Koh AS, Gao F, Leng S, Kovalik JP, Zhao X, Tan RS, Fridianto KT, Ching J, Chua SJ, Yuan JM, Koh WP, Zhong L. Dissecting Clinical and Metabolomics Associations of Left Atrial Phasic Function by Cardiac Magnetic Resonance Feature Tracking. Sci Rep. 2018 May 25;8(1):8138. doi: 10.1038/s41598-018-26456-8.
Results Reference
background
PubMed Identifier
28976207
Citation
Koh AS, Gao F, Liu J, Fridianto KT, Ching J, Tan RS, Wong JI, Chua SJ, Leng S, Zhong L, Keng BM, Huang FQ, Yuan JM, Koh WP, Kovalik JP. Metabolomic profile of arterial stiffness in aged adults. Diab Vasc Dis Res. 2018 Jan;15(1):74-80. doi: 10.1177/1479164117733627. Epub 2017 Oct 4.
Results Reference
background
PubMed Identifier
31418823
Citation
Keng BMH, Gao F, Teo LLY, Lim WS, Tan RS, Ruan W, Ewe SH, Koh WP, Koh AS. Associations between Skeletal Muscle and Myocardium in Aging: A Syndrome of "Cardio-Sarcopenia"? J Am Geriatr Soc. 2019 Dec;67(12):2568-2573. doi: 10.1111/jgs.16132. Epub 2019 Aug 16.
Results Reference
background
PubMed Identifier
30350416
Citation
Koh AS, Gao F, Tan RS, Zhong L, Leng S, Zhao X, Fridianto KT, Ching J, Lee SY, Keng BMH, Yeo TJ, Tan SY, Tan HC, Lim CT, Koh WP, Kovalik JP. Metabolomic correlates of aerobic capacity among elderly adults. Clin Cardiol. 2018 Oct;41(10):1300-1307. doi: 10.1002/clc.23016.
Results Reference
background

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Tackling Disruptions to Frailty Interventions: Developing Personalized Interventions Targeted for Older Persons With Cardiac Frailty

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