Profile of Pain and Unpleasant Sensations in Patients With Referred Pain

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-03-30

Study Completion Date

2019-07-31

Brief Summary

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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.

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Detailed Description

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Conditions

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Referred Pain Somatic Pain Neuropathic Pain

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients

Referred pain

Patients with referred pain

Intervention Type OTHER

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

Interventions

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Patients with referred pain

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

Intervention Type OTHER

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No