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Headache in Undergraduate Students and Biopsychosocial Status

NCT05843760 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 257

Last updated 2023-10-03

No results posted yet for this study

Summary

The primary aim of this study was to determine the prevalence of headache in undergraduate students. The frequency, duration, localizations and symptoms of headache will be determined with the information obtained as a result of the forms filled in by the participants.

The second aim of this study is to examine the effects of headache on physical, social and psychological status in undergraduate student(participants) from a biopsychosocial perspective.

Conditions

  • Headache Disorders, Primary
  • Prevalence
  • Migraine
  • Student
  • Psychosocial Problem

Interventions

OTHER

personal information form

undergraduate student(participants) will be asked; age, weight, height, smoking and alcohol use, and headache.

OTHER

headache-specific questionnaires

ıd migraine test, numeric rate scale, hit-6 headache impact test, headache information form

OTHER

Questionnaires for assessing biopsychosocial status

hospital anxiety depression, Discomfort Intolerance Test, pittsburgh sleep quality index, fatigue severity scale, self compassion scale, Body Awareness Questionarre, cervical range of motion, İnternational Physical Activity Questionnaire, 12-Item Short-Form Health Survey

Sponsors & Collaborators

  • şeyda öztürk

    lead OTHER

Principal Investigators

  • nezire köse, prof · HacettepeUniversity Faculty of Physical Therapy and Rehabilitation

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-04
Primary Completion
2023-06-02
Completion
2023-06-12

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05843760 on ClinicalTrials.gov