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Active, not recruitingNCT03071107FITNESSUpdated Jun 12, 2020

Frailty Intervention Trial in End-Stage Patients on Dialysis

An interventional study of Multi-disciplinary intervention in Hemodialysis Complication, Nutritional Deficiency and Physical Activity, sponsored by Adnan Sharif. Active, not recruiting at 1 site in United Kingdom. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-06-12.

Sponsored by Adnan Sharif · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Hemodialysis Complication
  • Nutritional Deficiency
  • Physical Activity
03

In context

Malnutrition

1,587 studies on the registry are indexed under Malnutrition; 237 are open to participants now.

This study's planned enrollment of 50 is below the median of 90 across 1,134 interventional studies indexed under Malnutrition.

Browse Malnutrition studies →

Lead sponsor

This is the only study on the registry with Adnan Sharif as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • On hemodialysis

Exclusion criteria

Exclusion Criteria:

  • Inability to give consent
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Active comparator
    Multi-disciplinary intervention arm

    Multi-disciplinary intervention on frailty parameters including input from dietitian, physiotherapist and medical team

    Behavioral: Multi-disciplinary intervention

  • No intervention
    Control arm

    Standard of care

Interventions

  • BehavioralMulti-disciplinary intervention

    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.

06

What researchers measure

Primary outcomes

  1. Feasibility of frailty intervention study in haemodialysis patients

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

    Time frame: 6-months

Secondary outcomes

  1. Change in frailty status

    Change in frailty score between baseline and end of study

    Time frame: 6-months

  2. Mortality

    Difference in mortality episodes between randomised arms

    Time frame: 6-months

  3. Hospitalisation

    Difference in episodes of hospitalisation between randomised arms

    Time frame: 6-months

07

Study locations

1 site
  • University Hospitals Birmingham NHS Foundation Trust
    Birmingham, West Midlands B15 2WB, United Kingdom
08

References and documents

Publications

  • 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. PubMed 30143028 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 12, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03071107
Lead sponsor
Adnan Sharif
Responsible party
Adnan Sharif (Chief Investigator, University Hospital Birmingham NHS Foundation Trust) — Sponsor-investigator
First posted
Mar 6, 2017
Start date
Dec 1, 2017
Primary completion
Jun 15, 2019
Completion
Aug 2025 (estimated)
Last update
Jun 12, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jun 2020. You cannot join it, but the record below documents what was studied.

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