Effect of Encouragement on Six Minute Walk Test Performance

Sponsor
University of Central Lancashire (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04586725
Collaborator
Coventry University (Other), University of Hull (Other), University of Salford (Other)
76
2
27

Study Details

Study Description

Brief Summary

Peripheral artery disease (PAD) is characterised by a build up of fatty plaque in the arteries in the lower limbs, resulting in a reduction of blow flow to the muscles. Globally, it is estimated that 236 million people are living with PAD. A classic symptom of PAD is intermittent claudication (IC) which is characterised by muscle cramps in the lower limbs, typically brought on by exercise and relieved at rest. Exercise is recommended at first line treatment for IC. However to assess IC symptoms in response to an exercise study, maximal walking capacity (the furthest they can walk before it becomes too painful to walk) is typically the main measure. A patients walking capacity is assessed by a number of exercise testing protocols including the six-minute walk test (6MWT), where patients walk for six minutes with the aim to walk as far as they can in the time allotted. Patient encouragement has been shown to improve walking performance by as much as 30 meters in heart failure and respiratory disease populations. However the effect of encouragement on walking performance in people with IC is yet to be studied.

Condition or Disease Intervention/Treatment Phase
  • Other: Encouragement a one minute intervals
  • Other: Encouragement a two minute intervals
N/A

Detailed Description

Peripheral artery disease (PAD) is characterised by atherosclerotic lesions of the arteries in the lower limbs, resulting in a reduction of blow flow (Hiatt, 2001). Globally, it is estimated that 236 million people are living with PAD, with the number of cases increasing by 24% from 2000 to 2010. A classic symptom of PAD is intermittent claudication (IC), characterised by ischemic muscle pain precipitated by exertion and relieved by rest. IC is associated with various comorbidities such as diabetes mellitus, hypertension and dyslipidaemia as well as reductions in physical function, quality of life, and balance. National and international guidelines recommend supervised exercise therapy as first line treatment for patients with IC.

To assess IC impairment in response to an exercise intervention, maximal walking capacity is typically the primary outcome in randomised controlled trials (RCT's). This involves a patient walking for as long as possible until ischemic leg symptoms, fatigue or other symptoms prevent them from continuing. This is assessed by a number of exercise testing protocols including the six-minute walk test (6MWT). The American Thoracic Society provide guidelines for performing a standardised 6MWT including verbal phrases that are conducted every minute. Conversely, Montgomery and Gardner suggest encouragement every two minutes. Encouragement has been shown to significantly affect walking performance by as much as 30 meters in heart failure and respiratory disease populations. However the effect of encouragement on walking performance in people with IC is yet to be investigated.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
76 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Masking:
Single (Participant)
Masking Description:
Participants will be blinded to the level of encouragement they will receive during the tests
Primary Purpose:
Treatment
Official Title:
The Effect of Encouragement on Six Minute Walk Test Performance in Patients With Intermittent Claudication
Anticipated Study Start Date :
Oct 1, 2021
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Jan 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Encouragement every minute

Patients will be randomised to six tests at one week apart

Other: Encouragement a one minute intervals
Patients will perform the six exercise tests with encouragement at one minute intervals

Other: Encouragement a two minute intervals
Patients will perform the six exercise tests with encouragement at two minute intervals

Active Comparator: Encouragement every two minutes

Patients will be randomised to six tests at one week apart

Other: Encouragement a one minute intervals
Patients will perform the six exercise tests with encouragement at one minute intervals

Other: Encouragement a two minute intervals
Patients will perform the six exercise tests with encouragement at two minute intervals

Outcome Measures

Primary Outcome Measures

  1. Maximal walking distance (MWD) [6 weeks]

    Metres walked during the tests

Secondary Outcome Measures

  1. Learning effect metres walked [6 weeks]

    To see if a learning effect exists between tests

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. 18 years old

  2. Resting ankle brachial pressure index (ABPI) <0.9 or a reduction of ≥ 20 mmHg following exercise testing (per site protocol)

  3. Able to walk unaided

  4. English speaking and able to follow exercise instructions

  5. Able to provide informed consent

Exclusion Criteria:
  1. Those who have critical limb threatening ischaemia (rest pain and/or tissue loss)

  2. Unable to provide consent

  3. Those presenting with any significant comorbidities or contraindications to exercise testing or training in accordance to the American College of Sports Medicine

  4. Uncontrolled or symptom limiting coronary heart or pulmonary disease

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Central Lancashire
  • Coventry University
  • University of Hull
  • University of Salford

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Stefan Birkett, Lecturer In Exercise Science, University of Central Lancashire
ClinicalTrials.gov Identifier:
NCT04586725
Other Study ID Numbers:
  • UCentalLancashire2
First Posted:
Oct 14, 2020
Last Update Posted:
Aug 4, 2021
Last Verified:
Jul 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 4, 2021