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Clinical Trials/ISRCTN13212899
ISRCTN13212899
Completed
未知

A parallel group, individually randomized clinical trial to evaluate the effect of a mobile phone application to improve sexual health among youth in Stockholm County

FORTE Swedish Research Council for Health, Working life and Welfare0 sites433 target enrollmentJune 22, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
FORTE Swedish Research Council for Health, Working life and Welfare
Enrollment
433
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

2018 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/29402241 protocol 2021 Results article in https://www.ncbi.nlm.nih.gov/pubmed/31628248 results (added 05/03/2020) 2020 Other publications in https://pubmed.ncbi.nlm.nih.gov/32012038/ Development of the Mobile Phone App (added 11/07/2023)

Registry
who.int
Start Date
June 22, 2017
End Date
June 30, 2019
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
FORTE Swedish Research Council for Health, Working life and Welfare

Eligibility Criteria

Inclusion Criteria

  • 1\. Youth aged 18\-23
  • 2\. Youth who own a smart phone
  • 3\. Youth who are sexually active (had at least two partners during the past six months). Added 16/10/2017: This criteria is to ensure youth included in the trial have recently had sex outside a stable relationship

Exclusion Criteria

  • Current exclusion criteria as of 20/11/2017:
  • 1\. Youth who do fulfil inclusion criteria
  • 2\. Youth who do not wish to participate
  • 3\. Women who only have sex with women will be excluded from the study as the interventions mainly focuses on safe sexual practices related to condom use
  • 4\. Close friend/sibling recruited into the trial
  • Exclusion criteria as of 05/09/2017:
  • 1\. Youth who do fulfil inclusion criteria
  • 2\. Youth who do not wish to participate
  • 3\. Women who only have sex with women will be excluded from the study as the interventions mainly focuses on safe sexual practices related to condom use
  • Previous exclusion criteria:

Outcomes

Primary Outcomes

Not specified

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