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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05620303
Other study ID # UCLMCFE00085
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 2, 2022
Est. completion date September 30, 2023

Study information

Verified date March 2023
Source University of Castilla-La Mancha
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effects of the Archena Infancia Saludable project on adherence to MD and 24-h movement behaviors in schoolchildren


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 154
Est. completion date September 30, 2023
Est. primary completion date July 31, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years to 13 Years
Eligibility Inclusion Criteria: Schoolchildren aged 6-13 years will be eligible Exclusion Criteria: - Participants with any pathology that contraindicate exercise or that request special attention. - Participants under pharmacological treatment that prevent them from receiving the contents of the activities of the program. - Participants or parents/legal guardians presenting Spanish learning difficulties. - Participants do not authorized by the parents/guardians to be included in the research project. - Participants do not agree to take part in the research project.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise
Parents/guardians will receive three different contents weekly (i.e., infographics, video recipes, information pills, or videos) each week related to 24-h movement behaviors (i.e., PA, sedentary behavior, sleep duration) or Mediterranean Diet for 36 weeks.

Locations

Country Name City State
Spain Colegio El Ope Murcia

Sponsors (1)

Lead Sponsor Collaborator
University of Castilla-La Mancha

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Other 24-h movement behaviors (self-reported) parents/guardians The level of physical activity and sitting time will be assessed by the International Physical Activity Questionnaire-short form (IPAQ-SF). From baseline to 36 weeks later.
Other Adherence to the Mediterranean diet (parents/guardians) Parents/guardians will be also administered a 17-item Mediterranean dietary questionnaire, a modified version of the previously validated questionnaire used in the PREDIMED trial designed to assess adherence to Mediterranean Diet. Meeting with each of the 17 items relating to characteristic food habits will be scored with zero or one point. Therefore, the total score will range from 0 to 17 points, with 0 points denoting no adherence to the MD and 17 meaning maximum adherence to the Mediterranean Diet. From baseline to 36 weeks later.
Other Anthropometrics measurements (parents/guardians) The body weight and body height of the parents/guardians will be self-reported. Body mass index (BMI) will be computed by dividing body weight (in kg) by the height (in squared meters). From baseline to 36 weeks later.
Primary Adherence to the Mediterranean diet To assess the adherence to the Mediterranean Diet, the Mediterranean Diet Quality Index for Children and Teenagers (KIDMED) index will be used. From baseline to 36 weeks later
Primary 24-h movement behaviors (accelerometers) sedentary time A tri-axial accelerometer (Actigraph GT3x, Pensacola, FL, USA) will be used to assess sedentary time over seven consecutive days. From baseline to 36 weeks later
Primary 24-h movement behaviors (self-reported) Self-report of physical activity levels and sedentary behaviors in youth will assessed by the Youth Activity Profile - Spain. In this questionnaire, a rating scale is used with a score from 1 to 5 in which, in the first two sections, "1" indicates low intensity and frequency of physical activity and "5" indicates high intensity and frequency of physical activity; while, in the third section, "1" indicates a low amount of sedentary behaviors and "5" an excess of them. From baseline to 36 weeks later
Primary 24-h movement behaviors (accelerometers) physical activity A tri-axial accelerometer (Actigraph GT3x, Pensacola, FL, USA) will be used to assess physical activity over seven consecutive days. From baseline to 36 weeks later
Primary 24-h movement behaviors (accelerometers) sleep duration A tri-axial accelerometer (Actigraph GT3x, Pensacola, FL, USA) will be used to assess sleep duration over seven consecutive days. From baseline to 36 weeks later.
Secondary Anthropometrics measurements The body weight of the schoolchildren will be measured using an electronic scale (with an accuracy of 0.1 kg) (Tanita BC-545, Tokyo, Japan), while height will be determined by a portable height rod with an accuracy of 0.1 cm (Leicester Tanita HR 001, Tokyo, Japan). Body mass index (BMI) will be calculated by dividing body weight (in kg) by the height (in squared meters). Furthermore, BMI z-score will be computed by the WHO age-specific and sex-specific thresholds. From baseline to 36 weeks later
Secondary Active transportation Active transportation to and from school is evaluated by a self-reported questionnaire (Mode and Frequency of Commuting To and From School Questionnaire). Participants were categorized as "active" if reported: =2 active travel days out of 5 school days (questions #1 and #2) and = 4 active travel trips out of 10 school trips per week (question #3). The usual mode of commuting to/from school was categorized as active when participants reported = 1 active travel per day out of 2 daily school trips (question #4). Those who were not categorized as "active commuting" were categorized as "passive commuting" users. From baseline to 36 weeks later
Secondary Resting blood pressure Resting blood pressure will be measured using an automated blood pressure monitor with a fittingly sized cuff (Omrom® EVOLV HEM-7600T-E, Health-care Co, Kyoto, Japan). First, schoolchildren will be seated in a quiet room for 10 min with their feet on the ground and their back supported. Two readings will be taken, with the second blood pressure reading taken five min after the first. The average of the two measurements for systolic blood pressure and diastolic blood pressure will be retained. Subsequently, mean arterial pressure will be computed by the following formula: diastolic blood pressure + [0.333 × (systolic blood pressure - diastolic blood pressure)]. From baseline to 36 weeks later
Secondary Sleep disorders Sleep disorders will be evaluated by the BEARS (B = Bedtime Issues, E = Excessive Daytime Sleepiness, A = Night Awakenings, R = Regularity and Duration of Sleep, S = Snoring) scale. Any questions that are answered positively indicate a sleep problem. From baseline to 36 weeks later
Secondary Health-related quality of life Health-related quality of life will be measured by Child Health Utility 9D (CHU9D). The CHU9D consists of 9 dimensions: worried, sad, pain, tired, annoyed, schoolwork/homework, sleep, daily routine, ability to join in activities with five different levels representing increasing levels of severity within each dimension. Furthermore, CHU9D scores will be used in cost-utility analyses. From baseline to 36 weeks later
Secondary Self-reported physical fitness Self-reported physical fitness will be assessed by the International Fitness Scale (IFIS), which is composed of a 5-point Likert-scale items asking about the children' perceived global physical fitness, cardiorespiratory fitness, muscular fitness, speed-agility, and flexibility in comparison with their counterparts' physical fitness (very poor (1), poor (2), average (3), good (4), and very good (5)). From baseline to 36 weeks later
Secondary Parents'/guardians' perception of their children's body mass index status This outcome will be evaluated with the following question: "In relation to his/her height, which of the following options best describes your child's weight: 1) substantially above normal, 2) slightly above normal, 3) normal, 4) below normal?". From baseline to 36 weeks later
Secondary Academic performance Academic records will be provided at the end of the academic year by the school. Firstly, academic performance will be evaluated according to the grade obtained in Language, Mathematics, Language and Mathematics (combined), English, as well as the grade point average of these three subjects. Secondly, academic performance will be assessed by computing the grade point average of all the subjects taken by the children. From baseline to 36 weeks later.
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