Digital Intervention

5

Review clinical trials related to Digital Intervention. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Advancing Precision Medicine for Cardiovascular Disease and Diabetes in Asian Populations: Digital Intervention Cohort

The overarching aim is to improve cardiometabolic health and promote healthy ageing by supporting adults to adopt favourable lifestyle patterns identified through our observational research. The trial will recruit n=600 to be involved in Phase I (referred to as the "Optimisation Phase") of a two-phase project (Phase II trial registration will be submitted separately). All participants will complete a baseline study visit where, after consent taking, will complete a baseline questionnaire, receive a smartwatch each and additional wearables if applicable, and download the study app for the receiving and testing of interventions and completion of short form surveys. Participants will be involved in the continual evaluation and optimisation of ecological momentary interventions (EMIs) in adaptive, factorial, micro-randomised trials over 12 months. Consenting participants may also be contacted to participate in interviews to be involved in the co-design of interventions, or to provide insights to the feasibility and process evaluation of the trial.

Participants needed: 600
Trial details
Age: 21-69Biological sex: AllType: InterventionalSponsor: National University of SingaporeUpdated: Jul 27, 2026Locations: 1
Eligibility criteria

are currently enrolled in the Singapore Population Health Studies - Multi-Ethnic... [+7]

have a history or current condition of stroke, heart attack, kidney failure, dia... [+6]

Status: Recruiting

Prospective Exploratory Study on the Comprehensive Application Effectiveness of Exercise Prescription Decision Support Tools in the Management of Patients With "Four Highs" (Hypertension, Hyperglycemia, Hyperlipidemia, Hyperuricemia)

This study conducted a six-month exploratory clinical trial to evaluate the impact of an exercise prescription mini-program, based on the "Exercise Guidelines for the 'Four Highs'", on the physical activity levels and related health indicators of patients with hypertension, hyperglycemia, hyperlipidemia, and hyperuricemia in primary healthcare settings in China.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: China National Center for Cardiovascular DiseasesUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Aged 18 years or older. [+4]

History or acute episode of cardiovascular or cerebrovascular disease, including... [+11]

Status: Recruiting

Usability Study of Gestational and Postpartum Weight Management Program

The principal aim of this study is to evaluate the usability of the Hope-D gestational and 6 months postpartum weight management program. We will evaluate the usability, functionality, and acceptability of the developed Hope-D weight management program that includes digital pathway for weight management, general or individual weight management plan and individual or group coaching for weight management from pregnancy to 6 months postpartum.

Participants needed: 30
Trial details
Age: 18-50Biological sex: FemaleType: ObservationalSponsor: Turku University HospitalUpdated: Dec 23, 2025Locations: 1
Eligibility criteria

General pregnant women with prepregnancy BMI at least 30 kg/m2 [+1]

Status: Not yet recruiting

A Digital Intervention to Improve Oral Health Practices

This study evaluates a 16-week parent-focused digital intervention to improve oral health practices in children aged 6-10 through daily reminders, quizzes, challenges, gamification, and behavior tracking, supported by an optional moderated WhatsApp group for peer engagement and motivation.

Participants needed: 800
Trial details
Age: 6-10Biological sex: AllType: InterventionalSponsor: Universiti Putra MalaysiaUpdated: Aug 24, 2025Locations: 4
Eligibility criteria

Parents or primary caregivers of children aged 6-10 years. [+4]

Children with serious medical conditions (e.g., immunodeficiency, congenital ano... [+3]

Status: Not yet recruiting

Testing and Comparing the Impacts of Mhealth-Based and Web-Based Education on Oral Cancer

Introduction: Oral cancer is a malignant neoplastic disease affecting the lip, oral cavity (mouth) and/or the oropharynx. Despite the intense and diverse public health interventions on oral cancer prevention, the global prevalence rates of oral cancer and its major risk factors are still very high. Hence, oral cancer is an issue of serious global health importance. Aim: To test and compare the effectiveness, usability, uptake, and acceptability of an educational website and a mobile health application prototype on oral cancer in improving oral cancer knowledge among university students. Methods: This study will adopt a randomised control trial design, and it will be conducted among 75 first-year bachelor's degree students from five universities across two continents: University of Rwanda (Rwanda, Africa), Usmanu Danfodiyo University (Nigeria, Africa), University of Peradeniya (Sri Lanka, Asia), University of Ibadan (Nigeria), and Saveetha University (India, Aisa). The study participants will be in three groups (Group 1, Group 2, and Group 3). The participants in Group 1 will be the control group (n = 25 participants; 5 participants from each university); that is the group that will not receive an educational intervention. However, those in Group 2 (n = 25 participants; 5 participants from each university) will receive a web-based educational intervention on oral cancer while those in Group 3 (n = 25 participants; 5 participants from each university) will receive an app-based educational intervention on oral cancer. Pretest survey and posttest survey will be done for all participants. The data collected will be statistically analysed using the Statistical Package for Social Sciences (SPSS) version 28 software. Descriptive statistics will be done for all variables while inferential statistics (analysis of variance) will be done to test for associations between variables of interest. Conclusion: The findings of this study will determine the effectiveness, usability, uptake, and acceptability of the tested digital intervention tools.

Participants needed: 75
Trial details
Age: 18-39Biological sex: AllType: InterventionalSponsor: University of RwandaUpdated: Dec 2, 2024Locations: 5
Eligibility criteria

being a first-year bachelor degree student of either University of Rwanda (Rwand... [+3]

being a member of staff or a visitor or a non-first year bachelor degree student... [+4]