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Clinical Trials/NCT07123610
NCT07123610CompletedNot Applicable

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

Bahçeşehir University1 site in 1 country130 target enrollmentStarted: May 8, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
130
Locations
1
Primary Endpoint
MEDAS Score

Study Overview

Brief Summary

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).

Detailed Description

Background Shift work misaligns endogenous circadian rhythms with environmental light-dark cycles, predisposing workers to poor sleep, metabolic dysregulation, weight gain and cardiometabolic disease. Observational and experimental evidence indicates that dietary patterns rich in plant foods, monounsaturated fats and lean proteins-exemplified by the Mediterranean diet (MedDiet)-can attenuate inflammation, improve lipid and glycaemic profiles, and enhance subjective well-being. Educational interventions that reinforce MedDiet principles may therefore represent a pragmatic, low-risk strategy to mitigate health risks in shift-working nurses.

Study Desing Design: Single-group, pre-post intervention study Setting: Private general hospital in Muğla, Türkiye Sample Size: 130 nurses (≈80 % women) employed in rotating shifts, aged 18-55 y Allocation: Not applicable (no comparison arm)

Participant Eligibility Inclusion Criteria Registered nurse working ≥3 rotating shifts per month at the study hospital Age 18-55 years Written informed consent Exclusion Criteria Pregnancy or lactation Current participation in another lifestyle or drug trial Diagnosed sleep disorder requiring pharmacotherapy Medical condition necessitating therapeutic diet incompatible with MedDiet principles Inability to attend ≥75 % of education sessions

Intervention Mediterranean Diet Education Programme (Weeks 1-4) Format: Four weekly face-to-face group sessions (60 min each) delivered by a registered dietitian trained in behavioural counselling.

Content:

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
18 Years to 55 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

  • •Pregnancy or lactation
  • •Current participation in another lifestyle or drug trial
  • •Diagnosed sleep disorder requiring pharmacotherapy
  • •Medical condition necessitating therapeutic diet incompatible with MedDiet principles
  • •Inability to attend ≥75 % of education session

Arms & Interventions

Shift working nurses

Experimental

Intervention: Mediterranean Diet Education Program (Behavioral)

Outcomes

Primary Outcomes

MEDAS Score

Time Frame: Baseline (week 0) and post-intervention (week 8)

Change in Mediterranean Diet Adherence Score (MEDAS) Change in adherence to the Mediterranean diet as measured by the 14-item Mediterranean Diet Adherence Screener (MEDAS). This validated questionnaire assesses the frequency and quality of consumption of key Mediterranean dietary components. Scores range from 0 to 14, with higher scores indicating greater adherence.

Secondary Outcomes

  • Change in Physical Activity(Baseline (week 0), Postintervention (week 8))
  • BMI Change(Baseline (Week 0) and Post-Intervention (Week 8))
  • Sleep Quality(baseline (week 0) postintervention (week 8))
  • Waist Hip Ratio(Baseline (Week 0) and Post-Intervention (Week 8))
  • Change in Blood Results Profile(Baseline (Week 0) and Post-Intervention (Week 8))

Investigators

Sponsor
Bahçeşehir University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ilayda Ozturk Altuncevahir

Assist. Prof.

Bahçeşehir University

Study Sites (1)

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