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Profile of Pain and Unpleasant Sensations in Patients With Referred Pain

Spatiotemporal Profile of Pain and Unpleasant Sensations in Referred Pain: a Feasibility Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03926364
Enrollment
90
Registered
2019-04-24
Start date
2018-03-30
Completion date
2019-07-31
Last updated
2019-08-21

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

Conditions

Neuropathic Pain, Referred Pain, Somatic Pain

Keywords

Pain drawings, referred pain, somatic pain, neuropathic pain, e-health, pain location, biopsychosocial factors, back pain, neck pain, pain extent, function

Brief summary

This feasibility study primarily aimed to assess the technology acceptance and usability of a pain tracking software in patients with spinally referred chronic pain. The secondary aim was to assess the fluctuations in pain intensity and distribution, using the pain tracking software during a 3-month period. Additionally, the study aimed to explore the patients' behavior when self-reporting pain when given the opportunity to use a variety of pain quality descriptors, such as tingling, burning and stabbing. Patients with spinally referred chronic pain will be recruited to participate. Participants will be asked to use a pain tracking software to create weekly pain reports for a 3-month period. These pain reports consist of pain drawings and intensity scales. Additionally, patients will complete baseline disability and pain catastrophizing online questionnaires. The project does not affect treatment or does not offer any intervention.

Interventions

OTHERPatients with referred pain

The project does not affect treatment or does not offer any intervention.

Sponsors

Aalborg University Hospital
CollaboratorOTHER
Aalborg University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Suffer from pain in the neck or lumbar spine referring to a limb for a more than 7 consecutive days * Participant is willing and able to give informed consent for participation in the study.

Exclusion criteria

* Pregnancy or breastfeeding, severe infections, cancer. * Epilepsy, Multiple sclerosis, history of stroke, diabetes, traumatic spinal cord injury resulting in permanent functions loss * Lack of ability to cooperate due to language barrier, cognition or inability to use technology.

Design outcomes

Primary

MeasureTime frameDescription
Change in pain extent for 3 months3 monthsChanges in pain extent as measured by the number of pixels drawn in digital pain drawings, at weekly intervals.

Secondary

MeasureTime frameDescription
Change in pain intensity for 3 months3 monthsChanges in usual and current pain intensity as measured by a Numerical Rating Scale, at a weekly interval.
Changes in pain location for 3 months3 monthsChanges of the location of pain measured by appearance and disappearance of pain in different body regions.
Disability levels at baselineBaselineDescription of disability levels as assessed by the Oswestry (if pain located in back) or the Neck Disability Index (if pain located in neck) online questionnaires.
Pain Catastrophizing scoreBaselineScores obtained from an online Pain Catastrophizing Scale (PCS) at baseline

Other

MeasureTime frameDescription
Demographic informationAt baselineOnline demographic information

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026