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Invitation to take part in survey;
Pacing using a Heart Rate Monitor

*This survey closed on 15 October 2021
Thank you to all who took part
You can read the results here

We are pleased to present "an international survey of experiences and attitudes towards Pacing using a heart rate monitor for people with Myalgic Encephalomyelitis / Chronic Fatigue Syndrome."

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People with ME often use heart rate monitors to pace their activities but there has been very little research exploring the use and peoples experiences of this approach.

 

The aim of this study is to explore the experiences of and attitudes towards pacing with a heart rate monitor in people with ME.

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How can I take part?

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The first step is to read the patient information sheet.

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The link to the survey can be found on the information sheet.

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Download Patient Information Sheet Here

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You can find out more about using a heart rate monitor on our website here.

*This survey closed on 15 October 2021
Thank you to all who took part*

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Physios for ME

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The information provided on this website is meant to inform and signpost helpful resources. Any treatment for a person with ME should always be individualised, monitored and regularly evaluated

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We do not provide clinical services, individual medical advice, or recommendations for private therapists

Contact

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Contact us at physiotherapyforme@gmail.com 

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