- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06100445
Exercise Engagement in People Over 60 at Risk of Falls
Barriers and Facilitators to Exercise Engagement in People Over 60 at Risk of Falls: an Exploratory Study
It is a qualitative study, using semi structured interviews to explore patient's experiences of falls and their perceptions on facilitators and barriers to exercise.
Aim: To explore reasons for and against engaging with exercises at home in participants over the age of 60 at risk of falls.
To explore:
- Patients' preferences to exercise format and type eg/ leaflet, online, access, such as the Chartered Society of Physiotherapy (CSP) chair exercises leaflet or individual personalized rehabilitation programme handouts
- The ability to discuss falls risk with health professionals.
- If health inequalities exist with people at risk of falls and exercising.
- Sustainability of exercise, in order to reduce the risk of falls in this population.
- The need to develop MSK internal and external facing falls management pathways.
Suitability: Patients over the age of 60, who have been identified at risk of falls, having been referred to MSK Physiotherapy in Rossendale.
'Risk of falls' is defined as: patient self-reports they are unsteady, had one or more fall in the last 6 months, or clinician identified a slow/unsteady gait pattern on examination.
Semi structured interviews on up to ten participants. It is anticipated that this sample size will give adequate data saturation. Approximately 12 months from participant recruitment to analysis of findings.
Study Overview
Status
Intervention / Treatment
Detailed Description
One in three people over the age of 65 and one in two over the age of 80 will fall each year. A fall is the main reason older people attend A and E. Falls can result in soft tissue injuries and broken bones, the most significant being a hip fracture, and these often require physiotherapy input. Locally, we have above average rates of hip fracture. Falling also reduces confidence and further mobility, which can also impact on developing long term health conditions.
Research has shown that exercise can help improve the strength and balance in people over 60 at risk of falls. Balance and strength exercises have been shown in previous research to reduce the risk of falls by 25% in patient's over 60. However, in other research, 78% of patients over the age of 75 have not done exercises at home in the last 5 years.
Exploring patient views on exercises and their physiotherapy experience will help us understand why patients engage or not with exercise and improve our services.
Patients who are at risk (identified through the EMIS template) of falls and have expressed an interest in being involved in research and who meet the additional eligibility criteria will be approached by the researcher. Eligible participants interested in participating will be contacted and sent the patient information sheet and consent form. They will be contacted within two weeks to see if they want to participate and assistance with the consent form either over phone or face to face.
A copy of the consent form will be scanned into the participant notes on EMIS, and paper copies stored securely in a locked filing cabinet.
All participants will have the opportunity to ask any questions regarding consent and the study prior to commencing the interviews and data collection.
The right of the participant to refuse to participate in research study without giving reasons will be respected. All participants are free to withdraw at any time without giving reasons and without prejudicing further treatment.
Face to face interviews will be recorded via an encrypted voice Dictaphone recorder. If conducting interviews via telephone call or MS teams, then voice recordings using the encrypted dictaphone will also be used. The interview will take approximately half an hour, and patients will only be interviewed once, there will be no follow up in this study.
All participant identifiable information will be kept confidential, and a participant number will be used. Recordings will be loaded onto a password protected secure trust server, accessible only to the researcher and the original recording deleted off the Dictaphone within 48 hours (about 2 days). Once transcribed, the recording on the drive will then be deleted.
Anonymised qualitative data will be transcribed by an NIHR transcriber. Then it will be analysed using thematic analysis using NVivo version 12, or the most up to date version of NVivo, a qualitative data analysis software. All data will be anonymised prior to analysis using an allocated participant ID number.
In the unlikely event that distress will be identified, the interview will be stopped, and the reason for the distress dealt with as per normal clinical practice. The participant will be given the option to stop participating (see withdrawal from participating below), or to continue with the interview at a later time. Participants can withdraw at any time up to once the interviews have been transcribed.
Data will then be used to improve patient services in physiotherapy, as well as highlight any service pathway and health inequality needs.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Michelle Thirlwall
- Phone Number: 01706 235398
- Email: michelle.thirlwall@elht.nhs.uk
Study Contact Backup
- Name: Michelle Stephens
- Phone Number: 07976152397
- Email: michelle.stephens@elht.nhs.uk
Study Locations
-
-
Lancashire
-
Blackburn, Lancashire, United Kingdom, BB2 3HH
- Recruiting
- East Lancashire Hospitals NHS Trust
-
Contact:
- Michelle Thirlwall
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Aged 60 years or over
- At risk of falls or had a fall due to a musculoskeletal cause (pain, muscle weakness, balance issue)
- Has capacity to consent, as deemed by the direct care team and researcher
- Can communicate in English OR the use of a translation service - Able to independently participate in an interview either face-to-face or via remote means OR can use a translation service
Exclusion Criteria:
- Aged under 60
- Have a medical cause of falls OR currently under investigation for a medical cause of falls (eg/ dizziness, cardiac, visual impairment reported as being the cause of the fall as opposed to weakness or pain in lower limbs/balance issues or unsteady on feet)
- Moderate to severe cognitive impairment impairing capacity to consent
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Explore reasons for and against engaging with exercises at home.
Time Frame: Through study completion, an average of 1 year
|
By identifying themes during anaylsis of study interviews
|
Through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patients' thoughts on service materials, provision and communication
Time Frame: Through study completion, an average of 1 year
|
Identify preferred exercise format and understanding of information eg/ leaflet, online, access, such as the Chartered Society of Physiotherapy (CSP) chair exercises leaflet or their own online personalised rehabilitation programme handouts by analysing themes of the interviews
|
Through study completion, an average of 1 year
|
Collaborators and Investigators
Collaborators
Investigators
- Study Chair: James Boateng, East Lancashire Hospitals NHS Trust
- Study Chair: Elizabeth Lightbody, National Institute for Health Research, United Kingdom
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DEV072
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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