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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02579785
Other study ID # MSI-007-14
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 19, 2015
Est. completion date July 15, 2016

Study information

Verified date February 2021
Source Marie Stopes International
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess whether a mobile phone intervention can be effectively used to improve post menstrual regulation contraceptive uptake and continuation in Bangladesh. The study will consist of two phases: Phase I: A formative phase to understand barriers to post-abortion contraceptive uptake and continuation and the content and modality of messages most appropriate for women in the study areas; and Phase II: An RCT will be conducted to test the effectiveness of the mHealth intervention developed during the formative phase on contraceptive use.


Description:

The proposed study aims to develop and evaluate a mHealth intervention to promote post-abortion contraceptive uptake and continuation among menstrual regulation clients in the Sylhet, Chittagong and Dhaka regions of Bangladesh. The aim of the formative phase of the study is to develop an interactive two-way messaging service for post-MR clients. The messaging service will deliver information relating to the women's contraceptive method of choice as well as information about other modern contraceptive methods. This part of the study will focus on determining the modality, content, timing, language and acceptability of messaging services for post menstrual regulation clients. The aim of the RCT phase is to measure the effect of mHealth on uptake or switching to long-acting reversible contraceptives at the 4 month and 12 month follow ups. The investigators expect mHealth to have a positive effect on uptake and a negative effect on discontinuation rates of contraceptive users.


Recruitment information / eligibility

Status Completed
Enrollment 972
Est. completion date July 15, 2016
Est. primary completion date July 15, 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 49 Years
Eligibility Inclusion Criteria: - Received menstrual regulation services using Manual Vacuum Aspiration (MVA) or Medical Abortion (MA) - Have a personal mobile telephone - Agree to receive messages on mobile about family planning - Provide informed consent for participation Exclusion Criteria: - Received anaesthesia for their MVA procedure - Intend to become pregnant within the next six months - Intend to use, or for partner to use, a permanent method of contraception (i.e. sterilisation) within the next six months

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mhealth intervention
A series of ten automated interactive voice messages will be delivered to the participant's mobile phone over a period of 4 months. Messages will be targeted to the method of contraception the participant is using (no-method, condoms, pills, injectable, implant, copper coil). Messages will support uptake of contraception among no-method users. Messages will support existing users to continue their method and to use it correctly and will also encourage participants who are not happy with their method to switch to a different method. All messages will end with five options: Press 1 to repeat the message, press 2 to listen to recorded information about methods of contraception, press 3 to speak to a counsellor, press 4 to tell me you're fine, press 5 to stop receiving these messages.

Locations

Country Name City State
Bangladesh Marie Stopes Bangladesh Maternity Clinic, Chittagong
Bangladesh Marie Stopes Clinic Brahman Baria Chittagong
Bangladesh Marie Stopes Clinic Chandpur, Comilla Chittagong
Bangladesh Marie Stopes Clinic Chittagong 1 Chittagong
Bangladesh Marie Stopes Clinic Comilla Chittagong
Bangladesh Marie Stopes Clinic Cox's Bazar Chittagong
Bangladesh Marie Stopes Clinic Shitakunda Chittagong
Bangladesh Marie Stopes Femi Maternity Clinic Chittagong
Bangladesh RHSTEP Bandarban Clinic Chittagong
Bangladesh RHSTEP Chittagong Medical College Hospital Chittagong
Bangladesh RHSTEP Clinic Khagrachhari Chittagong
Bangladesh RHSTEP Cox's Bazar Sadar Hospital Chittagong
Bangladesh RHSTEP Rangamati Sadar Hospital Chittagong
Bangladesh Faridpur Maternal and Child Welfare Centre Dhaka
Bangladesh Kishoreganj Maternal and Child Welfare Centre Dhaka
Bangladesh Manikganj Maternal and Child Welfare Centre Dhaka
Bangladesh Mari Stopes Clinic Manikgonj Dhaka
Bangladesh Marie Stopes Bashail Maternity Clinic Dhaka
Bangladesh Marie Stopes Clinic Balurmath Dhaka
Bangladesh Marie Stopes Clinic Gazipur Dhaka
Bangladesh Marie Stopes Clinic Kallyanpur Dhaka
Bangladesh Marie Stopes Clinic Kamrangirchar Dhaka
Bangladesh Marie Stopes Clinic Madaripur Dhaka
Bangladesh Marie Stopes Clinic Mymensingh Dhaka
Bangladesh Marie Stopes Clinic Sherpur Dhaka
Bangladesh Marie Stopes Clinic Tongi Dhaka
Bangladesh Marie Stopes Kadamtali Maternity Clinic Dhaka
Bangladesh Marie Stopes Premium 1 Clinic Dhaka
Bangladesh Marie Stopes Premium 2 Clinic Dhaka
Bangladesh Marie Stopes Referal Clinic, Tangail Dhaka
Bangladesh Mohammapur Fertility Services and Training Centre Dhaka
Bangladesh RHSTEP Dhaka Medical College Hospital Dhaka
Bangladesh RHSTEP Faridpur Medical College Hospital Dhaka
Bangladesh RHSTEP Mymensingh Medical College Hospital Dhaka
Bangladesh RHSTEP Sir Salaimullh Medical College Hospital Dhaka
Bangladesh Rupganj UHC Health Unit Dhaka
Bangladesh Marie Stopes Clinic Chatak Sylhet
Bangladesh Marie Stopes Clinic Moulvi Bazar Sylhet
Bangladesh Marie Stopes Sylhet Maternity Clinic Sylhet
Bangladesh RHSTEP Sylhet OAG Osmani Medical College Hospital Sylhet
Bangladesh Shreemongol UHC Health Unit Sylhet

Sponsors (3)

Lead Sponsor Collaborator
Marie Stopes International Ipas, London School of Hygiene and Tropical Medicine

Country where clinical trial is conducted

Bangladesh, 

Outcome

Type Measure Description Time frame Safety issue
Primary Use of long acting and reversible contraceptive at 4 months Proportion of subjects that self-report using a long acting and reversible contraceptive (coil or implant) 4 months
Secondary Use of long acting and reversible contraceptive at 2 weeks and 12 months Proportion of subjects that self-report using a long acting and reversible contraceptive (coil or implant) 2 weeks and 12 months
Secondary Use of any modern method at 2 weeks, 4 months and 12 months The proportion of subjects that self report using any effective modern contraceptive method: Modern contraceptive methods are defined according to the WHO as those associated with <10% 12 month pregnancy rates (WHO, 2011) 2 weeks, 4 months and 12 months
Secondary Pregnancy Proportion of subjects pregnant that self-report pregnancy at the time of follow-up 4 months and 12 months
Secondary Menstrual Regulation Proportion of subjects that self report having had an MR procedure since baseline 4 months and 12 months
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