SMS-based Summons in Cervical Screening

Sponsor
Karolinska Institutet (Other)
Overall Status
Recruiting
CT.gov ID
NCT04061967
Collaborator
Region Skane (Other)
20,000
6
1
129.4
3333.3
25.8

Study Details

Study Description

Brief Summary

Prevention of cervical cancer with cervical screening (gynecological cell test) is one of the most successful screening activities in medicine. In Sweden screening has taken place since the 1960s and prevented tens of thousands of women from having cervical cancer. There are strong reasons why it is especially important to promote that invitations to sampling really is reaching out. The women who regularly attend screening after the invitation reduce their risk of cervical cancer by as much as 90%. Of the women who currently have cervical cancer (about 550 women per year in Sweden), as many as 38% did not participate in the screening. Invitations for screening are sent to the entire population in Sweden aged 23-70. Current national estimate of how many in the population participating as recommended is 82.9% of the population. In addition, many women sometimes participate (they then get some reduced cancer risk). The highest cancer risk is among those women who have never participated as well as women who have had cell changes but have not participated. Cervical cancer is the first form of cancer for which there are approved molecular screening tests (HPV test). Unlike the older screening method (cytology), it works great to take a cervical sample at home if the sample is to be analyzed for HPV (the analysis method is so sensitive that it does not matter if the sample is not optimally taken).

Invitations and reminders about cervical screening are today sent out with physical letters (about 3 million letters per year in Sweden). These dispatches involve waste of resources and has a negative environmental impact. Regarding reminders, we have seen in previous research that the effect is not optimal. When sending a physical reminder letter to women who have not participated in more than 10 years (current routine), only 2% of the women recalled came for sampling. Reminders with SMS are now standard for many businesses in society, such as car testing or dental appointments. It is inexpensive, saves the environment and there are studies that suggest it is more effective than sending physical letters. In this study, we intend to investigate whether SMS reminders for screening lead to increased participation and thus to a higher proportion of detected, treatable precursors of cervical cancer compared to before.

Detailed Description

Non-participation in the cervical screening program is the main risk factor for cervical cancer. Therefore it is important to reduce barriers to screening and facilitate participation in the screening program of cervical cancer. Offering self-sampling kits for human papillomavirus (HPV) testing has been examined in several research studies as a way to reach women who have not responded to screening invitations.

The purpose of this study is to investigate whether SMS reminders for screening attendance will increase participation compared to the current method where reminders are sent out with physical letters. In this study, approximately 20,000 women with high risk of developing cervical cancer, due to not fully participating in screening, will be invited. The women receive an SMS offer to request a self-sampling kit via the internet. The self-sampling kit comes with an instruction on how to take the sample and a postage-free answer envelope.

Submitted samples are analyzed with an approved and accredited method (Cobas 4800, Roche) that analyzes for HPV 16, HPV18 and other carcinogens HPV types.

  1. For those women who are at the highest risk (previous glandular cell changes without follow-up), all HPV-positive women are referred via SMS directly to a women's clinic for investigation. HPV-negative women in this group have no increased risk and receive a text message with a calming message.

  2. Women of an age above the screening program but who have either had a cell change that is not followed up or who have not participated at all in the last 10 years are treated in the same way as in paragraph 1.

  3. Finally, the women of screening age who have not taken a cell sample for more than 15 years are identified. This group receive an SMS and HPV-positive women are referred, via SMS, for renewed sampling by a specially trained so-called dysplasia midwife. The sample is now being analyzed for both cytology and HPV. If the woman is HPV positive in both tests and in the case of deviating cytology, the woman is referred to a women's clinic. In other cases a text message with a reassuring message is sent.

The study has the usual level of confidence (p <0.05 two-sided) and statistical power (80%) the ability to demonstrate an increase of participation by 3 times or more.

The protocol will be piloted in the Region of Skåne in 2019 and then rolled out nationally in 2020.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20000 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Can SMS-reminders Result in Increased Participation in Cervical Screening?
Actual Study Start Date :
Aug 19, 2019
Anticipated Primary Completion Date :
Jun 1, 2030
Anticipated Study Completion Date :
Jun 1, 2030

Arms and Interventions

Arm Intervention/Treatment
Other: HPV self sampling test ordered

An invitation to order a HPV self sampling test through an online application will be sent by SMS

Other: Sending of screening summon.
A Cobas PCR Female swab sample packet will be sent. Response rates will be measured.
Other Names:
  • Response to screening summon.
  • Outcome Measures

    Primary Outcome Measures

    1. Proportion of women responding to summon [Measured from the date of the summons until 12 months after the summons]

      Participation rate in screening after summons.

    Secondary Outcome Measures

    1. Number of positive screens [Measured from the date of the summons until 12 months after the summons]

      Screening test results

    2. Rate of precursors of cancer [Measured from the date of the summons until 12 months after the summons]

      Cytologically and histopathologically confirmed percursors of cervical cancer.

    3. Rate of cancer [Measured from the date of the summons until 12 months after the summons]

      Histopathologically confirmed cervical cancers.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    33 Years to 75 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Women resident in Region Skane who either: 1) have had glandular cell transformation that has not been followed-up, 2) are older than 65 years and have had cell transformation that has not been followed-up or who have not participated in screening during the last 10 years, 3) women who have not been screened for more than 15 years.
    Exclusion Criteria:
    • No exclusion except those who do not consent.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Southern Region Lund Skåne Sweden 221 00
    2 Northern Region Umeå Västerbotten Sweden 901 87
    3 Western Region Gothenburg Västra Götaland Sweden 413 45
    4 Region of Stockholm-Gotland Stockholm Sweden 112 18
    5 Region of Middle Sweden Uppsala Sweden 751 85
    6 Southeast Region Linköping Östergötland Sweden 581 85

    Sponsors and Collaborators

    • Karolinska Institutet
    • Region Skane

    Investigators

    • Principal Investigator: Miriam Elfström, PhD, Karolinska Institutet

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Miriam Elfström, Affiliated Researcher, Karolinska Institutet
    ClinicalTrials.gov Identifier:
    NCT04061967
    Other Study ID Numbers:
    • 2019-03166
    First Posted:
    Aug 20, 2019
    Last Update Posted:
    Apr 22, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Miriam Elfström, Affiliated Researcher, Karolinska Institutet
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 22, 2022