German Translation and Cross-cultural Adaptation of the Headache Screening Questionnaire (HSQ) Followed by a Test-retest Reliability Study.

Migraine Clinical Trial

— GUR-HSQ  

Official title:

German Translation and Cross-cultural Adaptation of the Headache Screening Questionnaire (HSQ) Followed by a Test-retest Reliability Study.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05893004
• Other study ID #: GUR-HSQ
• Status: Recruiting
• Phase: N/A
• Start date: November 6, 2023
• Est. completion date: May 1, 2024

Study information

• Verified date: November 2023
• Source: Zurich University of Applied Sciences
• Contact: Ramon Gubser, Msc. student
• Phone: 076 360 40 55
• Email: gubsera1[@]students.zhaw.ch
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this study is to learn more about the Headache Screening Questionnaire in people with Headache. The main question is:

Does the lower limit of a 95% confidence interval of the HSQ in physiotherapy during a period of 2 to 4 weeks reach at least 0.4?

Description:

Data are collected using the REDCap web application (https://redcap.zhaw.ch/). REDCap is designed for the creation and administration of online surveys. Respondents can access the survey directly via a QR code or link and complete the screening questionnaire via smartphone or computer. In a first step, the participating persons are included or excluded based on the criteria mentioned (chapter: Proband:innen). Once eligibility has been confirmed, the HSQ is completed online for the first time in a second step. After that, the test persons will receive a reminder e-mail after 2 weeks to complete the retest online. After the reminder email the test persons have 2 weeks to complete the retest. Those who participate later will be excluded and not included in the data analysis. In addition, the retest asks whether the headaches have changed compared to the test due to the physiotherapeutic treatment. This is asked with a three Likert scale (not changed, slightly changed, strongly changed). The severely changed headaches are not included in the analysis.

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Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 31
• Est. completion date: May 1, 2024
• Est. primary completion date: March 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Individuals who are older than 18 years,

• live in Switzerland

• speak and understand German

• have had multiple headache episodes of the same or similar type

Exclusion Criteria:

• individuals with other known neurological conditions,

• known cognitive impairment

• known secondary headache types

Related Conditions & MeSH terms

• Headache
• Migraine
• Tension-Type Headache

Intervention

Diagnostic Test:
• Headache Screening Questionnaire
The Dutch Headache Screening Questionnaire (HSQ) is the only screening questionnaire based on ICHD-3 which has at least moderate confidence in its criterion validity according to GRADE. The HSQ has already been translated into Portuguese and validated5. The HSQ has only 8 items and requires little time to complete. Due to its good sensitivity, the HSQ screening questionnaire is particularly well suited to exclude migraine.

Locations

Country	Name	City	State
Switzerland	Zurich University of applied sciences	Winterthur

Sponsors (1)

Lead Sponsor	Collaborator
Markus J. Ernst

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Kappe Value	The HSQ uses nominal variables for screening the two primary headaches with defined cut-offs of 6 and 8 points for migraine and TTH, respectively. Therefore, for the test-retest reliability analysis, a Cohen's kappa with corresponding 95% confidence interval is calculated for both migraine and TTH.	Participants are assessed based on criteria (chapter: participants). Eligible individuals complete the HSQ online. A reminder email is sent after 2 weeks for the retest. Participants have 2 weeks to complete it. Late participants are excluded from analys