Preventing Eating Disorders by Improving Mental Health Literacy in Chinese Adolescents

Sponsor
Peking University (Other)
Overall Status
Completed
CT.gov ID
NCT05428046
Collaborator
(none)
1,395
1
2
6.5
213.4

Study Details

Study Description

Brief Summary

Mental health literacy (MHL) is necessary for the prevention, detection, and treatment of eating disorders, whereas the MHL about eating disorders is inadequate in China. Thus, the current study aimed to improve the MHL for eating disorders among Chinese adolescents via a brief online intervention.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: MHL intervention
  • Behavioral: Waiting list
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
1395 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Preventing Eating Disorders by Improving Mental Health Literacy in Chinese Adolescents: A Non-randomized Cluster Controlled Trial
Actual Study Start Date :
Nov 18, 2021
Actual Primary Completion Date :
Jun 5, 2022
Actual Study Completion Date :
Jun 5, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: MHL intervention

Mental health literacy intervention for eating disorder

Behavioral: MHL intervention
The current MHL intervention is a brief online intervention and comprises two modules. The first module is a short video introducing a teenage girl with bulimia nervosa. The second module is an online lecture comprising information about eating disorders including the prevalence, symptoms, type, cause, treatment, a related symptom checker, and sources of help. The above two modules are implemented in a single session lasting approximately 2 hours.

Other: Waiting list

The waiting list group received MHL intervention at the end of 12 weeks follow-up assessment.

Behavioral: Waiting list
Participants assigned to the waiting list group will not receive any intervention until the end of the 12 weeks follow-up. They received the same intervention as the MHL intervention group after the 12 weeks follow-up test.

Outcome Measures

Primary Outcome Measures

  1. Eating disorders mental health literacy [pre-intervention, post-intervention, 4 weeks follow-up, 12 weeks follow-up]

    The vignette for eating disorders mental health literacy was developed for the current study. The vignette describes a 14-year old girl who has bulimia nervosa. We also conducted a 5-point Likert scale to assess the knowledge, attitude, and help-seeking behaviors of eating disorders. Higer scores indicating a higer level of eating disorders mental health literacy.

  2. social distance scale [pre-intervention, post-intervention, 4 weeks follow-up, 12 weeks follow-up]

    The social distance scale was used to assess the level of social rejection that participants were likely to impose on people with eating disorders. The lower the score, the greater the desire for social distancing and the more negative the attitude toward people with eating disorders.

Secondary Outcome Measures

  1. Weight Concerns Scale [pre-intervention, post-intervention, 4 weeks follow-up, 12 weeks follow-up]

    The Weight Concerns Scale was used to assess weight concern and shape concern, with a higher score indicating more concerns.

  2. The SCOFF [pre-intervention, post-intervention, 4 weeks follow-up, 12 weeks follow-up]

    The SCOFF (Sick, Control, One, Fat, Food) was used to detect the existence of eating disorder symptoms. Scores of 2 or greater were originally set a cut-off point for maximum sensitivity to detect anorexia and Bulimia nervosa (Morgan et al, 1999).

  3. Actual help-seeking behavior [pre-intervention, post-intervention, 4 weeks follow-up, 12 weeks follow-up]

    We conducetd three items to assess the actual help-seeking behavior, including, "In the last 6 months, have you come into contact with someone who you think may have the same problems as Lily?","Have you offered help to them?", "How you helped him/her?".

  4. Patient Health Questionnaire-4 [pre-intervention, post-intervention, 4 weeks follow-up, 12 weeks follow-up]

    The Patient Health Questionnaire-4 was used to assess any negative impact on participant's well-being. Scores are rated as normal (0-2), mild (3-5), moderate (6-8), and severe (9-12). Total score ≥3 for first 2 questions suggests anxiety. Total score ≥3 for last 2 questions suggests depression.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Middle school students
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Peking University Beijing Beijing China 100871

Sponsors and Collaborators

  • Peking University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Peking University
ClinicalTrials.gov Identifier:
NCT05428046
Other Study ID Numbers:
  • MHL-ED
First Posted:
Jun 22, 2022
Last Update Posted:
Jul 7, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2022