Validation of Swedish Short PROM för Venous Insufficiency

Karolinska Institutet257 enrolled

Overview

Validation of a new short Swedish patient reported outcome measure for superficial venous insufficiency. Analysis of its capacity to measure quality of life and its responsiveness to change caused by treatment.

Study Type

OBSERVATIONAL

Enrollment

257

Conditions

Superficial Venous Insufficiency Quality of Life Change After Treatment

Interventions

patient reported outcome measureOTHER

2 questionnaires are tested against each other

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * agrees to participate, diagnosed with superficial venous insufficiency C2-C6 Exclusion Criteria: * does not want to participate, less than C2, does not submit the answered questionnaires

Locations (3)

Karlskoga venöst centrum

Karlskoga, Sweden

Åderbråckscentrum

Malmo, Sweden

Narvakliniken Åderbråck

Stockholm, Sweden

Outcomes

Primary Outcomes

the short PROM is valid for measurement of quality of life and detects change caused by treatment

Time frame: baseline and 8 weeks

Data from ClinicalTrials.gov

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