NCT06353308

Brief Summary

This paper presents the findings of a clustered randomized controlled trial (cRCT) that evaluated the effectiveness of an online feminist sexual health intervention among Chinese young adults, providing insights into the impacts of this innovative approach and contribute to the growing body of literature on feminist interventions for sexual health and equality promotion.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
422

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started May 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 12, 2023

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 10, 2024

Completed
21 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 2, 2024

Completed
26 days until next milestone

First Submitted

Initial submission to the registry

March 28, 2024

Completed
12 days until next milestone

First Posted

Study publicly available on registry

April 9, 2024

Completed
Last Updated

April 9, 2024

Status Verified

March 1, 2024

Enrollment Period

9 months

First QC Date

March 28, 2024

Last Update Submit

April 5, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Rape myth acceptance

    Illinois Rape Myth Acceptance Scale -Short Form, which consists of 17 items (1=not at all agree, 7=very much agree) assessing respondents' belief in rape myths (e.g., "Rape happens when a man's sex drive gets out of control"). The scores range from 17 to 119, with lower scores indicating less subscription to rape myths.

    From enrollment to the end of treatment at one week and three months

Secondary Outcomes (3)

  • Sociocultural Attitudes toward Appearance

    From enrollment to the end of treatment at one week and three months

  • Sexual Attitudes Scale

    From enrollment to the end of treatment at one week and three months

  • Sexual Desire Inventory

    From enrollment to the end of treatment at one week and three months

Study Arms (2)

General Sexual Health intervention

PLACEBO COMPARATOR

Participants will receive their general online sexual health education programming.

Behavioral: Sexual health intervention

Feminist Sexual Health Intervention

EXPERIMENTAL

Participants will receive online feminist sexual health program.

Behavioral: Sexual Violence Prevention

Interventions

The intervention included a game, five short videos, two posters, and five online quizzes, which were provided with a frequency of two posts per week and a final real-time online workshop. Materials included content on the spectrum of gender and sexual identities and orientations, gender and sexual roles, consent and communication, body positivity and self-acceptance, sexual pleasure and desire, as well as risky sexual behavior associated with dating app use and the legal issues and risks of sexual assault, such as precautionary steps and available resources.

Feminist Sexual Health Intervention

This general online sexual health education consisted of online videos, quizzes and game that covered a wide range of diverse topics on love, sex and relationships such as healthy and respectful relationships, body self-esteem, sexual identity and orientation, sexual rights and decision making, in addition to the conventional focus on sexual dysfunction and disease aversion.

General Sexual Health intervention

Eligibility Criteria

Age18 Years - 29 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Young adults aged between 18-29 years old who possessed a mobile phone
  • Had prior experience in using social media
  • Were able to read and understand Chinese

You may not qualify if:

  • \. Those with a physical impediment (e.g., blindness) preventing them from accessing the mobile content

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

The university of Hong Kong

Hong Kong, 000000, Hong Kong

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 28, 2024

First Posted

April 9, 2024

Study Start

May 12, 2023

Primary Completion

February 10, 2024

Study Completion

March 2, 2024

Last Updated

April 9, 2024

Record last verified: 2024-03

Locations