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Study Proposal for Web Based Intervention to Promote the Safe Usage of Dating Applications in Young Adults

Study Protocol for a Peer-led Web-based Intervention to Promote Safe Usage of Dating Applications Amongst Young Adults: A Cluster Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03685643
Enrollment
578
Registered
2018-09-26
Start date
2018-09-07
Completion date
2019-08-07
Last updated
2020-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adolescent Behavior, Behavior, Sex, Sex, Unsafe

Keywords

Peer-led, dating applications, young adults, sexual behavior

Brief summary

This study will evaluate the effectiveness of a program in promoting the safe usage of dating applications amongst young adults in Hong Kong. One group will receive the program regarding dating applications and the other group will receive a placebo program regarding health and exercise.

Detailed description

Dating applications are a popular platform to meet new people; however, they have been associated with risks such as unsafe sexual behavior and privacy concerns in young adults. The study design is an open-labeled cluster randomized controlled trial with an intervention and a placebo control arm. The intervention group will receive a web-based intervention developed through focus group discussions, crowdsourcing contest, and a Peer-Vetted Creative Production (PVCP) workshop comprising of four short videos, a risk assessment tool, and a scenario game. The control group will receive a web-based resource with similar multimedia elements on health and exercise. Based on the Information, Motivation, and Behavioral Skills (IMB) Model, the primary outcome of this study is self-efficacy in using dating applications measured by the General Self Efficacy Scale. Secondary outcomes include change in attitudes regarding risk perception measured by the Risk Propensity Scale and depression symptoms.

Interventions

BEHAVIORALIntervention - Dating application topic

The intervention will consist of multimedia content to promote the safe usage of dating applications and raise awareness of the risks associated with dating application usage. The intervention will be delivered one-time in a classroom setting.

BEHAVIORALControl - Health and exercise topic

The placebo control will consist of multimedia content regarding exercise and healthy living. It will be delivered once-time in a classroom setting.

Sponsors

The University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
17 Years to 27 Years
Healthy volunteers
Yes

Inclusion criteria

* 17-27 years old * Able to read and understand Chinese

Exclusion criteria

* Have a physical impediment (e.g. blindness) to prevent them from accessing the content

Design outcomes

Primary

MeasureTime frameDescription
Self Efficacy: This Will be Measured by the General Self Efficacy Scale8 monthsThe primary outcome will be the self-efficacy on the safe usage of dating. applications among young adults in Hong Kong. This will be measured by the General Self Efficacy Scale. The General Self Efficacy Scale is a 10-item scale (with 4 level Likert scale ranging from not true at all to exactly true) measuring one's self-belief in completing certain tasks or overcoming difficulties. The total score is calculated by finding the sum of all items with the total score ranging between 10 and 40, with a higher score indicating a higher level of self efficacy.

Secondary

MeasureTime frameDescription
Risk Taking Tendencies Will be Measured by the The Risk Propensity Scale.8 monthParticipants' risk taking tendencies will be measured by the The Risk Propensity Scale. It is a 9-item scale measuring general risk-taking tendencies. Each item is rated on a 9 level Likert scale (ranging from totally disagree to totally agree) with the final score ranging from 1-9. A higher score indicates higher risk-taking tendencies.
Depression Symptoms Will be Measured by the Patient Health Questionnaire-2 (PHQ-2).8 monthParticipants' risk of depression will be measured by the Patient Health Questionnaire-2 (PHQ-2). This is a 2 item scale (with a 4 level Likert scale ranging from Not at all to Nearly everyday) and the score ranges from 0-6, with a higher score indicating higher risk of depression.

Countries

Hong Kong

Participant flow

Pre-assignment details

A total of 578 eligible participants (290 in the intervention and 288 in the control) participated in the study.

Participants by arm

ArmCount
Intervention
The intervention materials were developed with high peer engagement and included four short videos, an interactive scenario game and a risk assessment tool.
276
Control
An existing website promoting physical activities and healthy living was served as a control.
266
Total542

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up1422

Baseline characteristics

CharacteristicInterventionTotalControl
Age, Customized
Age
19.83 years
STANDARD_DEVIATION 1.9
19.86 years
STANDARD_DEVIATION 1.85
19.88 years
STANDARD_DEVIATION 1.8
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
276 Participants542 Participants266 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
276 Participants542 Participants266 Participants
Race (NIH/OMB)
Black or African American
0 Participants0 Participants0 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
0 Participants0 Participants0 Participants
Region of Enrollment
Hong Kong
276 participants542 participants266 participants
Relationship Status
Others (Dating, marriage or cohabitating)
93 Participants189 Participants96 Participants
Relationship Status
Single
183 Participants353 Participants170 Participants
Sex: Female, Male
Female
139 Participants318 Participants179 Participants
Sex: Female, Male
Male
137 Participants224 Participants87 Participants
Sexual Orientation
Heterosexual
250 Participants490 Participants240 Participants
Sexual Orientation
Others (gay, lesbian or bisexual)
26 Participants52 Participants26 Participants
Types of housing
Private Apartment
107 Participants208 Participants101 Participants
Types of housing
Public housing estates
104 Participants186 Participants82 Participants
Types of housing
Short interim
5 Participants5 Participants0 Participants
Types of housing
Student Hostel
19 Participants48 Participants29 Participants
Types of housing
Subsided housing
34 Participants73 Participants39 Participants
Types of housing
Villiages
7 Participants22 Participants15 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 0
other
Total, other adverse events
0 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 0

Outcome results

Primary

Self Efficacy: This Will be Measured by the General Self Efficacy Scale

The primary outcome will be the self-efficacy on the safe usage of dating. applications among young adults in Hong Kong. This will be measured by the General Self Efficacy Scale. The General Self Efficacy Scale is a 10-item scale (with 4 level Likert scale ranging from not true at all to exactly true) measuring one's self-belief in completing certain tasks or overcoming difficulties. The total score is calculated by finding the sum of all items with the total score ranging between 10 and 40, with a higher score indicating a higher level of self efficacy.

Time frame: 8 months

ArmMeasureValue (MEAN)Dispersion
Intervention - Dating Application TopicSelf Efficacy: This Will be Measured by the General Self Efficacy Scale24.26 Score on a scaleStandard Deviation 5.48
Control - Health and Exercise TopicSelf Efficacy: This Will be Measured by the General Self Efficacy Scale22.30 Score on a scaleStandard Deviation 4.69
p-value: <0.001Wilcoxon (Mann-Whitney)
Secondary

Depression Symptoms Will be Measured by the Patient Health Questionnaire-2 (PHQ-2).

Participants' risk of depression will be measured by the Patient Health Questionnaire-2 (PHQ-2). This is a 2 item scale (with a 4 level Likert scale ranging from Not at all to Nearly everyday) and the score ranges from 0-6, with a higher score indicating higher risk of depression.

Time frame: 8 month

ArmMeasureValue (MEAN)Dispersion
Intervention - Dating Application TopicDepression Symptoms Will be Measured by the Patient Health Questionnaire-2 (PHQ-2).4.21 Score on a scaleStandard Deviation 1.46
Control - Health and Exercise TopicDepression Symptoms Will be Measured by the Patient Health Questionnaire-2 (PHQ-2).4.05 Score on a scaleStandard Deviation 1.33
p-value: 0.19Wilcoxon (Mann-Whitney)
Secondary

Risk Taking Tendencies Will be Measured by the The Risk Propensity Scale.

Participants' risk taking tendencies will be measured by the The Risk Propensity Scale. It is a 9-item scale measuring general risk-taking tendencies. Each item is rated on a 9 level Likert scale (ranging from totally disagree to totally agree) with the final score ranging from 1-9. A higher score indicates higher risk-taking tendencies.

Time frame: 8 month

ArmMeasureValue (MEAN)Dispersion
Intervention - Dating Application TopicRisk Taking Tendencies Will be Measured by the The Risk Propensity Scale.5.42 Score on a scaleStandard Deviation 1.23
Control - Health and Exercise TopicRisk Taking Tendencies Will be Measured by the The Risk Propensity Scale.5.59 Score on a scaleStandard Deviation 1.15
p-value: 0.12Wilcoxon (Mann-Whitney)

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026