Clinical trial · Interventional
Strategies to Improve the Experience of Gynaecological Screening
The First Visit for Gynaecological Screening - How do we Make it as Valuable as Possible?
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The aim is to evaluate different strategies to improve the experience and effect of the first visit for a cervical screening test (CST). 1. How do the context and the allotted time for the first visit for a CST affect women's i) experience of CST ii) knowledge of and attitudes towards CST and cervical cancer and iii) attitude towards contacting a midwife regarding sexual and reproductive health in the future 2. What effects do the RLP have, when used as a starting point for counselling at the first visit for a CST, on women's i) experience of CST ii) knowledge of and attitudes towards CST and cervical cancer iii) attitude towards contacting a midwife regarding sexual and reproductive health in the future and iv) knowledge of and attitudes towards fertility and preconception health Method: cluster randomised control trial evaluating the effect of different strategies, including RLP-based information, to improve the experience and effect of the first visit for a CST.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cervical Cancer | Malignant Cervical Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Changed clinical context | Other | — | UNRESOLVED |
| Extra time allotted | Behavioral | — | UNRESOLVED |
| RLP-information | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- NO_INTERVENTION
- label
- Group 1
- description
- Standard care for cervical screening test (CST) at the midwifery clinic (control group)
- type
- EXPERIMENTAL
- label
- Group 2
- description
- Standard care for CST at the youth clinic (intervention group 1)
- interventionNames
- Other: Changed clinical context
- type
- EXPERIMENTAL
- label
- Group 3
- description
- Standard care for CST at the youth clinic with extra time allotted (intervention group 2)
- interventionNames
- Other: Changed clinical context
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 23 Years
- Maximum age
- 23 Years
Show eligibility criteria text
Inclusion Criteria: * Persons with cervix * 23 years of age * Visiting midwife for their first cervical screening test Exclusion Criteria: * Non-Swedish-speaking
References
Publications (0)
Data not yet available