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NCT07123610Completed

Mediterranean Diet Education in Shift Nurses: Effects on Sleep, Activity, and Health Parameters

The Relationship Between Mediterranean Diet Education Given to Shift-Working Nurses and Sleep Quality, Physical Activity Level, Blood Parameters, and Anthropometric Measurements

Source: ClinicalTrials.gov · Last updated 14 Aug 2025

Brief summary (registry, in English)

This study aimed to evaluate the effects of Mediterranean diet education on sleep quality, physical activity levels, blood parameters, and anthropometric measurements among shift-working nurses. Primary outcomes: Change in Mediterranean diet adherence and sleep quality scores from baseline to post-intervention. Secondary outcomes: Changes in physical activity levels, anthropometric indices (e.g., BMI, waist-to-hip ratio), and blood parameters (fasting glucose, insulin, HOMA-IR, lipid profile).

Status (registry)
Completed
Study type
Interventional
Enrollment
130 (actual)
First submitted
31 Jul 2025
Start date
8 May 2024
Primary completion date
9 Nov 2024
Lead sponsor
Bahçeşehir University
NCT number
NCT07123610

What you commit to

  • Study type: Interventional
  • Participants enrolled: 130
  • From 8 May 2024 to the primary completion date, 9 Nov 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current participation in another lifestyle or drug trial

Other illness

  • Diagnosed sleep disorder requiring pharmacotherapy
  • Medical condition necessitating therapeutic diet incompatible with MedDiet principles

Other

  • Pregnancy or lactation
  • Inability to attend ≥75 % of education session

Who the study is looking for

  • Registered nurse working ≥3 rotating shifts per month at the study hospital
  • Age 18-55 years
  • Written informed consent

Age in the registry: 18 years to 55 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Bodrum Acıbadem Hospital
Coordinator of this site? Confirm its status
MuğlaTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.