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OpenTrials
Completed

NCT Number: NCT03269357

LARC Forward Counselling

Training of health care providers and structured LARC forward counseling may contribute to increased LARC uptake. The hypothesis to be tested is that by introducing LARC forward counselling an increase in LARC usage will be the result as well as decreased unplanned pregnancy and abortion. It is expected that the results of this study will highlight the importance of LARC forward counseling and thus provide the evidence needed to train health care providers and increase access to LARC in youth clinics, midwifery clinics and for post abortion contraception.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

WHO centre, Karolinska University Hospital

Stockholm, 17176, Sweden

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At risk for pregnancy (sexually active with men or anticipate becoming sexually active in the next 6 months).
  • Do not desire pregnancy .
  • No contraindications to LARC

Exclusion criteria

  • Undergone tubal ligation or other sterilization procedure.
  • Use of contraceptives for other purposes than contraception

Treatment and study plan

LARC forward structured contraceptive counselling

Other

Training of health care providers (HCPs), use of information material and counselling tools

Primary outcomes

  1. LARC prescriptions (recorded electronic prescriptions)

    Time frame: Evaluated at the index visit to the clinic

    The rate of women who receive a LARC prescription

Secondary outcomes

  1. LARC placements recorded in patient records

    Time frame: Evaluated at 3months follow up (FU)

    The rate of women who has a LARC method placed following the baseline visit

  2. Contraceptive method used reported by participants

    Time frame: Evaluated at 3,6 and 12 months FU

    The rate of women who use a contraceptive method

  3. Satisfaction with the chosen contraceptive method reported by participants

    Time frame: Evaluated at 3,6 and 12 months FU

    Satisfaction with the prescribed contraceptive method

  4. (Unplanned) pregnancy reported by participants and recorded in patient records

    Time frame: Evaluated at 3,6 and 12 months FU

    (Unplanned) pregnancy rate

Sponsors and collaborators

Lead sponsor

Kristina Gemzell Danielsson

Other

Registry information

Official study title

Effectiveness of LARC Forward Contraceptive Counseling: LOWE - A Cluster Randomized Intervention Project

Acronym: LOWE

Important dates

Study start
2017
Primary completion
2019
Study completion
2020
First posted
Aug 31, 2017
Registry last updated
Aug 18, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.