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Frailty, falls and the role of exercise in haemodialysis patients: a qualitative study

Understanding frailty, falls and the role of exercise in haemodialysis patients: A qualitative study (FLEX-HD)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN12840463
Enrollment
30
Registered
2017-05-11
Start date
2017-05-12
Completion date
Unknown
Last updated
2022-08-15

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

Conditions

Specialty: Renal disorders, Primary sub-specialty: Renal disorders

Interventions

Following enrolment in the study participants take part in three phases of qualitative data collection. Phase one: Pre-diary interview Semi-structured pre- interviews

Sponsors

University of Leicester
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Be a prevalent haemodialysis patient (receiving HD for 3 months or greater) 2. Age 18 years or older 3. Clinically stable at the time of recruitment 4. Able and willing to give informed consent 5. History of falls in the last 6 months or high risk of falls

Exclusion criteria

Exclusion criteria: 1. Unable or unwilling to give informed consent 2. Patients who are unable to understand, read or speak English 3. Unable to participate in an exercise due to perceived physical or psychological barriers 4. Unfit to undertake exercise or exercise testing according to the American College of Sports Medicine guidelines and as determined by the patient's Consultant Nephrologist including: 4.1. Significant ischaemia, recent myocardial infarction (2 weeks) or other acute cardiac event 4.2. Unstable angina 4.3. Uncontrolled cardiac dysrhythmias causing symptoms or haemodynamic compromise 4.4. Symptomatic severe aortic stenosis 4.5. Uncontrolled symptomatic heart failure 4.6. Acute pulmonary embolus or pulmonary infarction 4.7. Acute myocarditis or pericarditis 4.8. Suspected or known dissecting aneurysm 4.9. Acute systemic infection, accompanied by fever, body aches or swollen lymph glands

Design outcomes

Primary

MeasureTime frame
Experiences of patients will be explored using semi-structured qualitative interviews at baseline and around month four and solicited qualitative dairies kept between months one and three.

Secondary

MeasureTime frame
There are no secondary outcome measures.

Countries

England, United Kingdom

Contacts

Public ContactHannah Young
hannah.young@uhl-tr.nhs.uk+44 116 2584346

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 17, 2026