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Effectiveness and acceptability of a Sensiplan-based mobile phone app for family planning (FAB method)

Effectiveness and acceptability of a Sensiplan-based mobile phone app for family planning (FAB method) - SnApp

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00018866
Enrollment
275
Registered
2019-12-16
Start date
2021-05-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Z30

Interventions

Group 1: Use of the ladycycle app for the purpose of natural family planing at least for a year. Assessment of unexpected pregnancies and drop-out/lost-to-follow-up rate.

Sponsors

Sektion Natürliche Fertilität Universitätsfrauenklinik
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: We aim to recruit a study population of: - women, - age from 18-40 years - who are sexually active with a male partner - and agree to track their sexual behavior, - as well as their intention of family planning for the following cycle - who use the app Lady Cycle to avoid pregnancy and - who are willing to participate in the study for at least one year During this process - the participants must not take any sexual hormones and - at the time of entry to the study, the participants must not be pregnant NFP-beginners are defined as women, - who registered in the app less than three months ago - the data collection starts with the first cycle entered into the ladycycle app For postpartal, postabortal or postpill participants, - the first three cycles of the data collection will be dismissed to ensure a fertile population with risc exposure of an unplanned pregnancy. The study addresses especially women in German-speaking countries. Women in other countries with a different language are also allowed to participate in the study as long as the costs for the translation of the study documents are taken by the foreign counselling centres and a Sensiplan counseling service is available.

Exclusion criteria

Exclusion criteria: amenorrhea, known occlusion of oviduct, known OAT syndrome, known fertility disorders

Design outcomes

Primary

MeasureTime frame
Method-efficacy (perfect use rate acc. to Trussell) and use-effectiveness one year after the enrollment of the last participant (typical use, acc. to Kaplan Meier, cumulative life-table)

Secondary

MeasureTime frame
By determining the drop-out rates (cumulative life table acc. to Kaplan-Meier) for the reasons of the individual cancellation of the study participation, the acceptability of the app will be evaluated.

Countries

Australia, Austria, Belgium, Germany, Ireland, New Zealand, Switzerland, United Kingdom, United States

Contacts

Public ContactPetra Blim

Universitätsfrauenklinik, Gynäkologische Endokrinologie und Fertilitätsstörungen

petra.blim@med.uni-heidelberg.de06221 56-7856

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026