Frailty Intervention Trial in End-Stage Patients on Dialysis (FITNESS)
Primary Purpose
Hemodialysis Complication, Nutritional Deficiency, Physical Activity
Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Multi-disciplinary intervention
Sponsored by
About this trial
This is an interventional supportive care trial for Hemodialysis Complication
Eligibility Criteria
Inclusion Criteria:
- On hemodialysis
Exclusion Criteria:
- Inability to give consent
Sites / Locations
- University Hospitals Birmingham NHS Foundation Trust
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Multi-disciplinary intervention arm
Control arm
Arm Description
Multi-disciplinary intervention on frailty parameters including input from dietitian, physiotherapist and medical team
Standard of care
Outcomes
Primary Outcome Measures
Feasibility of frailty intervention study in haemodialysis patients
Feasibility of undertaking a full scale clinical intervention trial targeting frail haemodialysis patients
Secondary Outcome Measures
Change in frailty status
Change in frailty score between baseline and end of study
Mortality
Difference in mortality episodes between randomised arms
Hospitalisation
Difference in episodes of hospitalisation between randomised arms
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03071107
Brief Title
Frailty Intervention Trial in End-Stage Patients on Dialysis
Acronym
FITNESS
Official Title
Frailty Intervention Trial in End-Stage Patients on Dialysis: A Feasibility Study
Study Type
Interventional
2. Study Status
Record Verification Date
June 2020
Overall Recruitment Status
Active, not recruiting
Study Start Date
December 1, 2017 (Actual)
Primary Completion Date
June 15, 2019 (Actual)
Study Completion Date
August 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Adnan Sharif
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
The proposed investigation for this study aims to; 1) understand the prevalence and outcomes associated with frailty among haemodialysis patients; 2) ascertain the best frailty assessment tool for haemodialysis patients, and; 3) design a clinical study to explore the feasibility of facilitating, recruiting and executing a multi-disciplinary clinical and psychological intervention to improve frailty status among haemodialysis patients.
Work package 1: Firstly, there is a need to understand the prevalence and spectrum of frailty in a UK haemodialysis cohort and what impact frailty has for haemodialysis patients. To investigate this, the investigators will approach every patient on haemodialysis within the local catchment of haemodialysis units and, after informed consent, clinically phenotype their frailty status (pre- and post-haemodialysis for calculation of variability). The frailty phenotyping will encompass a number of frailty assessments (including the Edmonton Frail Scale, Clinical Frailty Scale from Rookwood score and Fried Frailty scale) to identify the ideal frailty assessment tool. All patients in this observational cohort study will be prospectively monitored for clinical/biochemical outcomes using an informatics-based approach for up to 60 months.
Work package 2: Building upon the work conducted in work package 1, work package 2 will aim to recruit 50 patients clinically phenotyped with pre-frailty from work package 1 into a feasibility study exploring a multi-disciplinary intervention to improve frailty status. Eligible patients, after informed consent, will be randomised into active or passive intervention. The active intervention will involve a dietitian and physiotherapist who have been trained and accredited with cognitive behavior intervention, utilising established behavioral intervention frameworks, to deliver a multi-disciplinary clinical intervention targeting multiple components of frailty.
The FITNESS project will therefore answer some important unanswered questions regarding frailty among the haemodialysis population and help in the design of a large multi-disciplinary intervention study if deemed feasible.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemodialysis Complication, Nutritional Deficiency, Physical Activity
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Multi-disciplinary intervention arm
Arm Type
Active Comparator
Arm Description
Multi-disciplinary intervention on frailty parameters including input from dietitian, physiotherapist and medical team
Arm Title
Control arm
Arm Type
No Intervention
Arm Description
Standard of care
Intervention Type
Behavioral
Intervention Name(s)
Multi-disciplinary intervention
Intervention Description
Participants in the intervention group will receive a multifactorial, interdisciplinary, treatment program intended to target pre-frailty for a 4-month period following randomization (physical meetings at 2-monthly time points with telephone consultations between meetings). The interventions will be individually tailored to each participant based on their frailty characteristics at baseline and amended if other problems are identified during the intervention program. This intervention team will consist of a renal dietitian and physiotherapist, both of whom will be trained and accredited in behavioural therapy intervention skills, and will focus on improving nutritional status and physical strength through resistance exercise training. They will be supported by a Clinical Research Fellow who will provide additional medical assessment to determine any reversible medical causes of frailty.
Primary Outcome Measure Information:
Title
Feasibility of frailty intervention study in haemodialysis patients
Description
Feasibility of undertaking a full scale clinical intervention trial targeting frail haemodialysis patients
Time Frame
6-months
Secondary Outcome Measure Information:
Title
Change in frailty status
Description
Change in frailty score between baseline and end of study
Time Frame
6-months
Title
Mortality
Description
Difference in mortality episodes between randomised arms
Time Frame
6-months
Title
Hospitalisation
Description
Difference in episodes of hospitalisation between randomised arms
Time Frame
6-months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
On hemodialysis
Exclusion Criteria:
Inability to give consent
Facility Information:
Facility Name
University Hospitals Birmingham NHS Foundation Trust
City
Birmingham
State/Province
West Midlands
ZIP/Postal Code
B15 2WB
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30143028
Citation
Anderson BM, Dutton M, Day E, Jackson TA, Ferro CJ, Sharif A. Frailty Intervention Trial iN End-Stage patientS on haemodialysis (FITNESS): study protocol for a randomised controlled trial. Trials. 2018 Aug 24;19(1):457. doi: 10.1186/s13063-018-2842-x.
Results Reference
derived
Learn more about this trial
Frailty Intervention Trial in End-Stage Patients on Dialysis
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