Completed

Patient Experience of Interventional Pain Management. Qualitative Study

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What is being collected

Data Collection

Other
Who is being recruted

Neurologic Manifestations+2

+ Pain

+ Signs and Symptoms

See all eligibility criteria
How is the trial designed

Other

Utilizing specific methods not covered by standard models in order to address unique research questions.
Observational
Study Start: April 2013
See protocol details

Summary

Principal SponsorEques Indolor AB
Last updated: January 31, 2018
Sourced from a government-validated database.Claim as a partner

Study start date: April 1, 2013

Actual date on which the first participant was enrolled.

A qualitative interview is performed with patients that have passed through an interventional pain management program. The transcribed interviews are analyzed with qualitative content analysis according to Graneheim and Lundman in order to illuminate the experience, feelings and thoughts arisen among the patients.

Principal SponsorEques Indolor AB
Last updated: January 31, 2018
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

19 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Other

Some studies use unique or mixed approaches that don't fit standard categories. These may include innovative observational methods or studies tailored to specific research questions.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neurologic ManifestationsPainSigns and SymptomsPathological Conditions, Signs and SymptomsChronic Pain

Criteria

Inclusion Criteria: Patients passed through an interventional pain management program Exclusion Criteria: Purposeful sampling will be applied

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Smärtkliniken Eques Indolor

Vallentuna, SwedenOpen Smärtkliniken Eques Indolor in Google Maps
CompletedOne Study Center