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The effects of exercise on experimentally induced pain-pressure threshold; a randomised repeated measure study in healthy participants.

The effects of exercise on experimentally induced pain-pressure threshold; a randomised repeated measure study in healthy participants.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20161107001
Enrollment
30
Registered
2016-11-07
Start date
2016-11-07
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Persistent pain healthy participants persistent pain pain threshold high intensity exercise

Interventions

This session will consist of 30 minutes of continuous cycling. The workload will be set at 35% of peak power achieved during the VO2peak test ,High Intensity Exercise: The session will consist of a 3&
minute warm up completed at 50 Watts&#44
followed by 10 × 60&#45
seconds high&#45
intensity cycle efforts interspersed with 60&#45
seconds of recovery after each. The workload during each interval will be set at 80% of peak power achieved during the VO2peak test
Moderate Intensity Training (MIT),High Intensity Training (HIT)

Sponsors

Teesside University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 50 Years

Inclusion criteria

Inclusion criteria: Healthy (self-report) and free from all exclusion criteria, Teesside University students and staff of Teesside University, aged between 16-50 years of age. An upper age limit has been included as preclinical studies have suggested that anatomical changes and increases in inflammation which occur due to increased age can lead to increased sensitivity to EIPPT (Yezierski, 2012). This is not considered to be discriminatory as it is methodologically justified.

Exclusion criteria

Exclusion criteria: People with any symptoms of or known presence of heart disease or major atherosclerotic cardiovascular disease, condition or injury or co-morbidity affecting the ability to undertake exercise, diabetes mellitus, early family history of sudden cardiac death and pregnancy or likelihood of pregnancy, any condition which could alter pain sensitivity such as neuropathic disorders, persistent pain, any present (or history, over the preceding six months) of medical problems of the upper limb, taking any analgesic medication (prescription or non-prescription), inability to, or any doubt of ability to, give Informed Consent.

Design outcomes

Primary

MeasureTime frame
experimentally induced pain-pressure threshold immediatly pre and post intervention Wagner Force Oneâ„¢ FDIX digital pressure algometer

Secondary

MeasureTime frame
not applicable not applicable not applicable

Countries

UK

Contacts

Public ContactCormac Ryan

Teesside University

c.ryan@tees.ac.uk00441642

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026