search
Back to results

Optimising the Efficacy, Patient Perception and Uptake of an Exercise Programme in People in Intermittent Claudication (SEIC)

Primary Purpose

Vascular Disease, Intermittent Claudication

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Supervised exercise programme
Sponsored by
Hull University Teaching Hospitals NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Vascular Disease focused on measuring Exercise

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with IC not referred for surgery
  • Community dwelling adults aged forty five or over
  • Ankle brachial index ABPI less than 0.9 at rest or a drop of more than 20 after exercise testing
  • Ability to walk unaided
  • English speaking and able to understand simple protocol instructions

Exclusion Criteria:

  • Participants who are unable to provide informed consent
  • Severe cardiovascular, musculo-skeletal or pulmonary illness precluding participation in the supervised exercise
  • Critical limb ischaemia
  • Active treatment for cancer

Sites / Locations

  • Hull Royal Infirmary

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Exercise

Arm Description

only 1 arm to trial

Outcomes

Primary Outcome Measures

Patient maximum walking distance

Secondary Outcome Measures

Full Information

First Posted
August 25, 2015
Last Updated
July 29, 2019
Sponsor
Hull University Teaching Hospitals NHS Trust
Collaborators
University of Hull
search

1. Study Identification

Unique Protocol Identification Number
NCT02641418
Brief Title
Optimising the Efficacy, Patient Perception and Uptake of an Exercise Programme in People in Intermittent Claudication
Acronym
SEIC
Official Title
Optimising the Efficacy, Patient Perception and Uptake of an Exercise Programme in People in Intermittent Claudication
Study Type
Interventional

2. Study Status

Record Verification Date
July 2019
Overall Recruitment Status
Completed
Study Start Date
May 2015 (undefined)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
October 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hull University Teaching Hospitals NHS Trust
Collaborators
University of Hull

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Peripheral arterial disease is a result of atherosclerotic occlusion in the major arteries supplying the lower limbs and is associated with an increased risk of mortality and morbidity. It results in restricted blood flow to the skeletal muscles causing intermittent claudication (IC). IC presents as cramp like pain affecting 5% of the population >50 years and is associated with a substantial reduction in walking capacity, quality of life and diminished physical function. Supervised exercise programmes have been demonstrated to improve maximum walking distances and NICE recommends group-based supervised exercise for treating patients with IC. However, there is significant variability in the impact of treatment across studies and little agreement on the underlying mechanism whereby exercise increases functional outcomes. Potential mechanisms include skeletal muscle metabolism, VO2 max, anaerobic threshold and endothelial function. Studies are needed to better understand how exercise improves outcome and in whom, so as to better refine and target the treatment. The participation of patients with IC in exercise programmes is low. The investigators need to understand factors influencing participation so that we can improve the number of patients with IC benefiting from the programme The research consists of two workstreams: Workstream one Objective: Assess the extent to which patient baseline characteristics and candidate physiological mechanisms are associated with clinical improvement in IC patients participating in an exercise programme Patients: Patients with documented IC referred from a Vascular Consultant. Eligible patients will be invited to participate in a 12 week supervised exercise programme. Testing Schedule: Measurements will be recorded at baseline (prior to exercise), immediately after the completion of the exercise programme and then three months after. Measurements include: Baseline characteristics that might predict outcome: Quality of life using the VascuQol questionnaire Clinical indicators of lower limb function: Ankle brachial pressure index (ABPI), intermittent claudication distance (ICD), Maximum walking distance (MWD). Candidate physiological mechanisms Aerobic capacity (VO2 max & AT) Muscular strength and endurance Muscle morphology (including muscle thickness, pennation angle, fascicle length and elastography) Endothelial function (sheer stress response as measured by flow mediated dilation) Analysis: Regression analysis will be used to explain variation in patient maximum walking distance at 3 months. The regression will use 9 candidate measures of physiological response and 3 baseline measures to explore what mechanism and patient factors may be associated with clinical improvements. 100 patients recruited over 2 years will give a 90% power to detect an additional increase in variability in MWD explained by each candidate measure of around 5% at the a 0.05 significance level. This research will be used to identify which types of exercise may be most influential in improving outcome and in which patients. Workstream two Objective: Explore the reasons behind patients' participation, non-participation in, experience of and adherence to the exercise programme. Study Design: An interview study of patients with IC routinely referred for supervised exercise. Three groups of patients will be invited to participate. Those who: Choose not to participate in the exercise programme (Group A) Agree to participate in the exercise programme (Group B). Agree to participate but discontinue after at least one session (Group C). Semi-structured face-to-face interviews with 20 patients per group, interviews will be conducted using a topic guide to ensure consistency. The format will be flexible to allow participants to generate naturalistic data on what they consider as important and / or successful in terms of outcome. Data will be analysed thematically and managed using Nvivo software - the approach will be inductive and iterative. This research will be used to redesign the current exercise programme to improve participation and so the impact of exercise in patients with IC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Disease, Intermittent Claudication
Keywords
Exercise

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
109 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise
Arm Type
Other
Arm Description
only 1 arm to trial
Intervention Type
Other
Intervention Name(s)
Supervised exercise programme
Intervention Description
supervised exercise programme
Primary Outcome Measure Information:
Title
Patient maximum walking distance
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with IC not referred for surgery Community dwelling adults aged forty five or over Ankle brachial index ABPI less than 0.9 at rest or a drop of more than 20 after exercise testing Ability to walk unaided English speaking and able to understand simple protocol instructions Exclusion Criteria: Participants who are unable to provide informed consent Severe cardiovascular, musculo-skeletal or pulmonary illness precluding participation in the supervised exercise Critical limb ischaemia Active treatment for cancer
Facility Information:
Facility Name
Hull Royal Infirmary
City
Hull
State/Province
East Riding Of Yorkshire
ZIP/Postal Code
HU3 2JZ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30583899
Citation
Harwood AE, Totty JP, Pymer S, Huang C, Hitchman L, Carradice D, Wallace T, Smith GE, Chetter IC. Cardiovascular and musculoskeletal response to supervised exercise in patients with intermittent claudication. J Vasc Surg. 2019 Jun;69(6):1899-1908.e1. doi: 10.1016/j.jvs.2018.10.065. Epub 2018 Dec 21.
Results Reference
result
Links:
URL
https://www.ncbi.nlm.nih.gov/pubmed/30583899
Description
Cardiovascular and musculoskeletal response to supervised exercise in patients with intermittent claudication.

Learn more about this trial

Optimising the Efficacy, Patient Perception and Uptake of an Exercise Programme in People in Intermittent Claudication

We'll reach out to this number within 24 hrs