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Clinical Trials/NCT03071107
NCT03071107UnknownNot Applicable

Frailty Intervention Trial in End-Stage Patients on Dialysis: A Feasibility Study

Adnan Sharif2 sites in 1 country50 target enrollmentStarted: December 1, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
50
Locations
2
Primary Endpoint
Feasibility of frailty intervention study in haemodialysis patients

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Supportive Care
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • On hemodialysis

Exclusion Criteria

  • Inability to give consent

Outcomes

Primary Outcomes

Feasibility of frailty intervention study in haemodialysis patients

Time Frame: 6-months

Feasibility of undertaking a full scale clinical intervention trial targeting frail haemodialysis patients

Secondary Outcomes

  • Change in frailty status(6-months)
  • Hospitalisation(6-months)
  • Mortality(6-months)

Investigators

Sponsor
Adnan Sharif
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Adnan Sharif

Chief Investigator

University Hospital Birmingham NHS Foundation Trust

Study Sites (2)

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