Effects of motor imagery on pain and itch perception
Official title: Investigation of the Neurophysiological and Psychological Aspects of Itch
Run by Aalborg University · NCT06503523 · Data updated 2026-11-12
This study tests if imagining movements can help reduce pain and itch sensations in people experiencing these feelings.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 60 Years |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Aalborg University Academic / other |
| Locations | 2 sites (Gistrup and 1 other locations) |
| Status | Recruiting |
| Started | October 1, 2024 |
| Main results expected | December 31, 2025 |
| Study ends | December 31, 2026 |
| Registry record updated | November 9, 2026 |
| Trial ID | NCT06503523 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are healthy men and women aged 18-60 who can speak and understand English.
✕Probably not a fit
Patients with a history of neurological, immunological, musculoskeletal, cardiac, or psychiatric disorders may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This project investigates how performing a motor imagery task influences cortical excitability during acute muscle pain and itch induced by different stimuli. The study aims to determine if motor imagery can mitigate the changes in cortical excitability associated with these sensations, which have overlapping neurophysiological mechanisms. Participants will undergo experimental pain and itch models while their cortical responses are measured using transcranial magnetic stimulation. The findings could enhance our understanding of pain and itch management.
Why it matters
Potential benefit: If successful, this study could provide new insights into non-pharmacological interventions for managing pain and itch.
How similar studies have gone: Previous studies have shown that motor imagery can positively influence pain perception, but its effects on itch are less understood, making this approach somewhat novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Healthy men and women * 18-60 years * Speak and understand English Exclusion Criteria: * Pregnancy or lactation * Drug addiction defined as any use of cannabis, opioids, or other addictive drugs * Previous or current history of neurological (e.g. neuropathy), immunological (e.g. asthma, immune deficiencies, arthritis), musculoskeletal (e.g. muscular pain in the upper extremities,), cardiac disorder (e.g., heart stroke), or psychiatric diagnoses (e.g. depression) that may affect the results * Current use of medications that may affect the trial, such as antihistamines, antipsychotics, and painkillers, as well as systemic or topical steroids * Skin diseases (e.g., atopic dermatitis, pruritus nodularis, eczema, psoriasis) * Moles, scars, or tattoos in the area to be treated or tested. * Consumption of alcohol or painkillers 24 hours before the study days and between these * Acute or chronic pain * Unable to pass the "Transcranial Magnetic Stimulation Adult Safety Screen" (subproject 1 and 2) * Contraindications to transcranial magnetic stimulation (TMS) application (history of epilepsy, metal implants in head or jaw, etc.) * Presence of implanted hearing aids or metal implants on the face, including permanent makeup or tattoos * Participation in other trials within one week of study entry (four weeks in the case of pharmaceutical trials) * Lack of ability to cooperate
Where it's running
-
Aalborg University
Gistrup, Denmark Recruiting -
Aalborg University
Gistrup, Denmark Recruiting
Study contacts
- Study coordinator: Silvia Lo Vecchio
- Email: slv@hst.aau.dk
- Phone: 21397785
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Topical Roflumilast Cream for Itch in Atopic Dermatitis: See If It Helps Over 4 Weeks
This trial tests whether a 0.15% topical roflumilast cream can reduce itching in people 12 years and older with mild to moderate atopic dermatitis over 4 weeks.
-
Exploring How Contagious Itch Works on the Skin
This study tests how itch spreads when histamine, cowhage, or a placebo are applied to the forearms to see how people feel itch and pain.
-
Placebo effects on histamine and cowhage-induced itch
This one-time, 1½-hour session will test whether applying a harmless cream reduces histamine- and cowhage-induced itch in healthy adults aged 18–60.
-
Mapping itch and pain receptor locations on the face
We will test how itch and pain are felt at different spots on the face in healthy adults by applying mild provocations (histamine, cowhage, capsaicin) and measuring responses over three days.
-
Using Virtual Reality and Hypnosis to Reduce Chronic Itch
This study is testing whether using virtual reality combined with hypnosis can help people with chronic itch feel better.
-
Blocking IL-13 to see how it changes itch and skin pain sensitivity
This trial will test whether lebrikizumab, a drug that blocks IL-13, changes itch and skin pain sensitivity in healthy adults and people with atopic dermatitis.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.