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Strategies to Improve the Experience of Gynaecological Screening

NCT05131581 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 206

Last updated 2025-01-14

No results posted yet for this study

Summary

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

Interventions

OTHER

Changed clinical context

Changed clinical context: from midwifery clinic to youth clinic

BEHAVIORAL

Extra time allotted

Extra time allotted for each visit for CST

BEHAVIORAL

RLP-information

Midwife-initiated discussion of the Reproductive Life Plan

Sponsors & Collaborators

  • Sophiahemmet University

    collaborator OTHER

  • Sormland County Council, Sweden

    collaborator OTHER

  • Uppsala University

    lead OTHER

Principal Investigators

  • Jenny Stern, PhD · Uppsala University

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
23 Years
Max Age
23 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-01
Primary Completion
2023-06-19
Completion
2023-06-19

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05131581 on ClinicalTrials.gov