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NCT04780633
PRECEDE-PROCEED Model-based Program on Genital Hygiene Behaviors
NA trial testing Precede-Proceed based Training Program on Genital Hygiene Behaviors in Genital Infection Female in 120 participants. Completed in 15 October 2017.
30 September 2017
Quick facts
| Lead sponsor | Ataturk University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | supportive care |
| Enrollment | 120 |
| Start date | 15 June 2017 |
| Primary completion | 30 September 2017 |
| Estimated completion | 15 October 2017 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Precede-Proceed based Training Program on Genital Hygiene Behaviors
Conditions studied
- Genital Infection Female — all drugs for Genital Infection Female →
Sponsor
Ataturk University
Who can join
Adults 18 to 49, female only, with Genital Infection Female. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The study was conducted to investigate the effect of a training program based on the PRECEDE-PROCEED Model on improving genital hygiene behaviors.It was carried out using experimental research design with pre-test and post-test, randomized and a control group. The study was conducted at Erzurum Saltuklu Family Health Center between June 2017 and January 2018. Of the women with genital infections, 120 women were included in the study, of which 60 were in the experimental group and 60 were in the control group. The data were collected by "Personal Information Form," "Genital Hygiene Knowledge, Attitude and Beliefs, Questionnaire" and "Genital Hygiene Behavior Inventory". In study, genital hygiene training intervention prepared according to the Precede-Proceed model was applied to the women in the experimental group. The women in the experimental group were measured at three different times: pre-test before training, post-test through training completition, and follow-up test after 4 weeks. The women in the control group did not receive any training intervention, the pre-test at the first encounter in the family health center and the post-test 5 weeks later.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04780633 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Ataturk University
- Last refreshed: 3 March 2021
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