Acceptability of Depo-subQ in Uniject

NCT ID: NCT01667276

Last Updated: 2013-07-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

476 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-07-31

Study Completion Date

2013-04-30

Brief Summary

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This is an observational study to assess the experience of current depot medroxyprogesterone acetate (DMPA) intramuscular (IM) clients and providers when they try Depo-subQ in Uniject and offer recommendations for the introduction of this method.

Detailed Description

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This is an observational study to assess the experience of current depot medroxyprogesterone acetate (DMPA) intramuscular (IM) clients and providers when they try Depo-subQ in Uniject and offer recommendations for the introduction of this method.

A total of 560 participants will be enrolled in the study in the following groups:

360 participants (120 in Uganda and 240 in Senegal) who are current DMPA IM clients who seek re-injection of DMPA from either community health workers (CHWs) or clinic-based providers; and are 18-40 years of age; received their most recent DMPA injection no more than 13 weeks prior to enrollment in the study \[16\].

Up to 100 participants (50 in Uganda and 50 in Senegal) current DMPA IM clients who meet the inclusion/exclusion criteria but do not want to receive the injection with Depo-subQ in Uniject and are willing to complete a short questionnaire

80 CHWs (40 in Uganda and 40 in Senegal) and 20 clinic-based providers (from Senegal only) who are trained to give Depo-subQ in Uniject as part of this study

Conditions

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Contraception

Study Design

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Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Age 18-40
* In general good health (the participant verbally reports she feels well)
* Using DMPA continuously for at least six months prior to enrollment in the study (i.e., had at least two previous injections)
* Received their most recent DMPA injection no more than 13 weeks prior to enrollment in the study at the study clinic or from a family planning provider involved in the study (Senegal only)
* Received their most recent DMPA injection no more than 13 weeks prior to enrollment in the study from a family planning provider involved in the study (Uganda only)
* Desires to be re-injected with DMPA
* Willing to sign an informed consent document
* Willing to provide contact information and be interviewed three months after enrollment.
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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United States Agency for International Development (USAID)

FED

Sponsor Role collaborator

PATH

OTHER

Sponsor Role collaborator

FHI 360

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Holly Burke, PhD, MPH

Role: PRINCIPAL_INVESTIGATOR

FHI 360

Anthony Mbonye, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Ministry of Health, Uganda

Bpcar M Daff, MD, PhD, MSc

Role: PRINCIPAL_INVESTIGATOR

Division de la Sante de la Reproduction

Locations

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Ministry of Health Clinics

All Cities Where There Is A Clinic, , Senegal

Site Status

Ministry of Health Clinics, Uganda

All Cities Where There Is A Clinic, , Uganda

Site Status

Countries

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Senegal Uganda

References

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Burke HM, Mueller MP, Perry B, Packer C, Bufumbo L, Mbengue D, Mall I, Daff BM, Mbonye AK. Observational study of the acceptability of Sayana(R) Press among intramuscular DMPA users in Uganda and Senegal. Contraception. 2014 May;89(5):361-7. doi: 10.1016/j.contraception.2014.01.022. Epub 2014 Feb 6.

Reference Type DERIVED
PMID: 24631328 (View on PubMed)

Burke HM, Mueller MP, Packer C, Perry B, Bufumbo L, Mbengue D, Daff BM, Mbonye A. Provider acceptability of Sayana(R) Press: results from community health workers and clinic-based providers in Uganda and Senegal. Contraception. 2014 May;89(5):368-73. doi: 10.1016/j.contraception.2014.01.009. Epub 2014 Jan 21.

Reference Type DERIVED
PMID: 24576792 (View on PubMed)

Other Identifiers

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10196

Identifier Type: -

Identifier Source: org_study_id

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