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Clinical Trials/NCT06404619
NCT06404619
Completed
Not Applicable

Impact of mHealth Implementation Program on Improving Nursing Students' Lifestyle: A Randomized Controlled Trial

Princess Nourah Bint Abdulrahman University1 site in 1 country220 target enrollmentAugust 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Lifestyle
Sponsor
Princess Nourah Bint Abdulrahman University
Enrollment
220
Locations
1
Primary Endpoint
Sleep quality scale.
Status
Completed
Last Updated
last year

Overview

Brief Summary

Healthy lifestyles are crucial for preventing chronic diseases. This study evaluated the effectiveness of mHealth intervention program in adopting healthy lifestyles.

Detailed Description

Healthy lifestyles are crucial for preventing chronic diseases. Nonetheless, approximately 90% of university students regularly engage in at least one unhealthy lifestyle. Mobile smart devices-based health interventions (mHealth) that incorporate theoretical frameworks regarding behavioral change in interaction with the environment may provide an appealing and cost-effective approach for promoting sustainable adaptations of healthier lifestyles. The aim of this study was to evaluate the effectiveness of mHealth intervention program compared to traditional (face-to-face) program in adopting healthy lifestyles among students of the Faculty of Nursing.

Registry
clinicaltrials.gov
Start Date
August 1, 2023
End Date
December 31, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shaherah Andargeery

Principal Investigator

Princess Nourah Bint Abdulrahman University

Eligibility Criteria

Inclusion Criteria

  • male or female nurse student
  • aged 19-24 years
  • with BMI ≥ 18.5
  • capable of performing physical activity
  • owner of a smartphone
  • ready to use different social media

Exclusion Criteria

  • on diet regimen or have a history of diet regimen
  • with history of chronic diseases e.g., DM, hypothyroidism or other endocrinal diseases
  • with history of medications that may cause weight gain e.g., antipsychotics, antidepressants, antiepileptics or steroids
  • with mental or psychological disorders

Outcomes

Primary Outcomes

Sleep quality scale.

Time Frame: Assessed just before and immediately after the intervention

It assesses the quality of sleep for the last one month and consists of 28 questions with four Likert scale (rarely, sometimes, often, and almost always). The total score can range from 0 to 84, with higher scores demoting more more frequent sleep disturbances (Good quality of sleep ≤ 28, Fair 29 - ≤ 56, and poor \> 56).

Physical activity time and levels of participants as assessed by Global/International Physical Activity Questionnaire (GPAQ/IPAQ).

Time Frame: Assessed just before and immediately after the intervention

The total weekly time spent on physical activity and the time spent in each domain (work, transportation, and recreational time) are determined by multiplying the number of days per week in each category by the average daily duration. Minutes per week in each category are then multiplied by metabolic equivalents (MET). The overall GPAQ score is described as "Low" if \< 600 MET-minutes/week, "Moderate" if = 600-1500 MET-minutes/week, or "High" if \> 1500 MET-minutes/week.

Dietary assessment using Food frequency questionnaire (FFQ).

Time Frame: Assessed just before and immediately after the intervention

It consists of 140 food items categorized under 27 categories with three Likert scale (usually eat, sometimes eat, and rarely eat). Score of 27-45 indicates bad healthy choices, 46-63 indicate fair healthy choices, and 64-81 indicate good healthy choices.

Secondary Outcomes

  • The weight in kilograms and height in meters will be combined to report the body mass index (BMI) in kg/m2.(Assessed just before and immediately after the intervention)
  • Blood Pressure Level assessed with the sphygmomanometer.(Assessed just before and immediately after the intervention)

Study Sites (1)

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