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Increasing condom use in STI clinic clients: Promoting the formation of Implementation Intentions to overcome the discrepancy between motivation and action.

Increasing condom use in STI clinic clients: Promoting the formation of Implementation Intentions to overcome the discrepancy between motivation and action. - Implementation Intentions and condom use

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON32185
Enrollment
180
Registered
2008-11-04
Start date
2009-11-02
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

STD

Interventions

The intervention is self-administered and will be conducted on a designated stand-alone personal computer placed in a private space of the clinic. After providing informed consent and adequate expla
Sheeran, Abraham & Orbell, 1999) they want to get some advice and form a plan which will help them to actually use condoms. Subsequently, these questions will result in the formulation of an *If-th

Sponsors

Universiteit Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Participation is voluntary and based on informed consent and potential participants have to be able to provide informed consent. Also, as the study and intervention will be conducted on a personal computer, participants need to feel competent in basic computer skills. Note that only minimal computer skills are required relating to the use of keyboard and mouse to enter responses and continue in the program. Furthermore, considering that the formation of Implementation Intentions is a method to promote acting on good intentions, the target population consists of individuals who intend to use condoms, but who have failed to act on that intention.

Exclusion criteria

Exclusion criteria: Clients who are younger than the legal age of consent or who can otherwise not provide informed consent are excluded from the study. Also excluded are individuals who are in a monogamous relationship for three months or more and individuals who do not intend to use condoms (more often).

Design outcomes

Primary

MeasureTime frame
The main parameter/endpoint of the study is the frequency of condom use for penetrative vaginal or anal sex in the three months after the intervention. This behavioural follow-up will be conducted online, via the Internet.

Secondary

MeasureTime frame
Not applicable.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)