IBI-HTA: Lifestyle Internet-Based Intervention On Hypertensive Patients With Overweight Or Obesity

Sponsor
Cardenal Herrera University (Other)
Overall Status
Completed
CT.gov ID
NCT04426877
Collaborator
(none)
135
1
2
5.1
26.5

Study Details

Study Description

Brief Summary

This study aims to analyze the effects of a 3 months duration self-applied online program, composed of 9 modules focused on promoting healthy lifestyle habits (healthy eating and increased physical activity), on obese or overweight adults with hypertension. Participants will be recruited from a hypertension unit of a public hospital. These patients will be randomized allocated into two interventional groups: experimental group will receive audiovisual instructions from their hypertension specialist doctor, and the control group from a doctor outside the patient. Assessment will include: body composition (BMI), blood pressure, levels of physical activity, functional capacity, fall risk, and quality of life.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Experimental group
  • Behavioral: Control group
N/A

Detailed Description

Hypertension and obesity or overweight related, even other associated comorbidities, involve a worrying public health problem. The evidence shows that healthy eating and regular physical exercise, monitored by different means (internet, face to face, exercise diaries), play an important prevention role to maintain health while ageing. In this way, Information and Communication Technologies (ICTs) have been demonstrated as a useful tool to promote health, working on barriers at the same time, such as low motivation and difficulties to maintain regular exercise or healthy eating habits. ICTs also allows to reach a wider audience at a lower cost, due to their good cost-benefit relationship and the possibility of increasing the efficiency of interventions. Therefore, this study aims to analyze the effects of a 3 months duration self-applied online program, composed of 9 modules focused on promoting healthy lifestyle habits (healthy eating and increased physical activity), on obese or overweight adults with hypertension. Participants will be recruited from a hypertension unit of a public hospital. These patients will be randomized allocated into two interventional groups: experimental group will receive audiovisual instructions from their hypertension specialist doctor, and the control group from a doctor outside the patient. Assessment will include: body composition (BMI), blood pressure, levels of physical activity, functional capacity, fall risk, and quality of life.

Study Design

Study Type:
Interventional
Actual Enrollment :
135 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Impact Of An Exercise And Nutritional Education Self-Applied Online Intervention On Body Composition And Blood Pressure On Hypertensive Adults With Overweight Or Obesity.
Actual Study Start Date :
Jan 1, 2021
Actual Primary Completion Date :
Jun 1, 2021
Actual Study Completion Date :
Jun 5, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

The experimental group will receive access to the web-based lifestyle intervention (exercise and nutritional education), supported by audiovisual instructions given by their hypertension specialist doctor.

Behavioral: Experimental group
The self-applied online program will comprise a three months behavioural intervention composed by 9 modules seeking to develop gradually achieving the goals of changing eating and physical activity habits, supported by audiovisual instructions. This group will receive access to the web-based lifestyle intervention (exercise and nutritional education), supported by audiovisual instructions given by their hypertension specialist doctor.

Experimental: Control Group

The control group will receive the same web-based lifestyle intervention (exercise and nutritional education), but in this case supported by audiovisual instructions given by a doctor outside the patient.

Behavioral: Control group
The self-applied online program will comprise a three months behavioural intervention composed by 9 modules seeking to develop gradually achieving the goals of changing eating and physical activity habits, supported by audiovisual instructions. This group will receive the same web-based lifestyle intervention (exercise and nutritional education), but in this case supported by audiovisual instructions given by a doctor outside the patient.

Outcome Measures

Primary Outcome Measures

  1. BMI [At three months]

    Body mass index

Secondary Outcome Measures

  1. Blood Pressure (BP) [At three months]

    Systolic and diastolic blood pressure

  2. Physical activity [At three months]

    Levels of physical activity (measured with SHORT-IPAQ Questionnaire). This Questionnaire measure assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives are considered to estimate total physical activity in MET-min/week and time spent sitting.

  3. Fall risk [At three months]

    Fall risk perception (measured with FES Questionnaire). The 'Falls Efficacy Scale' (FES) directly evaluate the impact of fear of falling on social life. This scale has excellent reliability, is correlated with measures of balance and gait, and predicts future falls and decline in functional capacity. The 16 items of the FES are rated according to "how concerned you are about the possibility of falling", using the following responses (score in parentheses): not at all (1), somewhat (2), fairly (3), and very concerned (4). Thus, the total score ranges from 16 to 64 points. Higher values indicate less fall-related self-efficacy (and more concern about falling).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Hypertension

  • Overweight or obesity (25 ≤ BMI ≤ 35 kg/m2)

  • Aged between 18-75 years

Exclusion Criteria:
  • Not having access to the Internet or lack of information about it.

  • Treatment with more than 3 antihypertensive drugs.

  • Meet the criteria of the DSM-IV-TR of a Food Disorder.

  • Presenting some type of severe psychiatric disorder.

  • Disability that prevents or hinders physical exercise.

  • Receiving some treatment for weight loss.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Enrique Rodilla Sala Sagunt Valencia Spain 46520

Sponsors and Collaborators

  • Cardenal Herrera University

Investigators

  • Principal Investigator: JUAN FRANCISCO L PÁRRAGA, PhD, Cardenal Herrera University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Juan F. Lisón Párraga, Dr, Head of Medicine, Cardenal Herrera University
ClinicalTrials.gov Identifier:
NCT04426877
Other Study ID Numbers:
  • UNIVERSITY CARDENAL HERRERA-85
First Posted:
Jun 11, 2020
Last Update Posted:
Jun 29, 2021
Last Verified:
Jun 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Juan F. Lisón Párraga, Dr, Head of Medicine, Cardenal Herrera University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2021