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Mobile Technology for Improved Family Planning (MOTIF)

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2014 by Marie Stopes International.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT01823861
First Posted: April 4, 2013
Last Update Posted: May 28, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
London School of Hygiene and Tropical Medicine
Information provided by (Responsible Party):
Marie Stopes International
  Purpose

An individual randomised controlled trial (RCT) to evaluate the effectiveness of a voice-based mobile phone health (mHealth) intervention to support post-abortion family planning (PAFP) at four Marie Stopes International clinics in Cambodia.

The study seeks to address the research question: does a PAFP mHealth intervention increase use of contraception in Cambodia?


Condition Intervention
Contraception Post-abortion Family Planning mHealth Behavioral: Mobile phone-based intervention

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Supportive Care

Resource links provided by NLM:


Further study details as provided by Marie Stopes International:

Primary Outcome Measures:
  • Use of a reliable contraceptive method at four-months post-abortion [ Time Frame: 4 months ]
    Self-reported use of pill, coil, implant or injection for all participants. Objective measurement of contraceptive use for participants from one clinic.


Secondary Outcome Measures:
  • Pregnancy [ Time Frame: 4 months ]
  • Repeat abortion [ Time Frame: 4 months ]
  • Contraceptive discontinuation [ Time Frame: 4 months ]

Enrollment: 500
Study Start Date: May 2013
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: September 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Mobile phone-based intervention
Standard care plus automated voice message to support post-abortion contraception use every two weeks for total of three months and direct follow up phone call by family planning counsellor depending on response to voice message.
Behavioral: Mobile phone-based intervention
Automated voice message to support post-abortion contraception use every two weeks for total of three months. Direct follow up phone call by family planning counsellor depending on response to voice message.
No Intervention: Standard care
Face-to-face post-abortion family planning (PAFP) counselling, follow-up at one or two weeks, clinic phone number, existing 'Hotline' phone number.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Client attending for abortion
  • Client does not want to have a child at the current time
  • Client aged 18 or over
  • Client owns a mobile phone
  • Client willing to receive simple voice messages relating to contraception from Marie Stopes in Khmer language

Exclusion Criteria:

  • Not meeting inclusion criteria
  • Declined to participate
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01823861


Locations
Cambodia
Marie Stopes International
Phnom Penh, Cambodia
Sponsors and Collaborators
Marie Stopes International
London School of Hygiene and Tropical Medicine
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Marie Stopes International
ClinicalTrials.gov Identifier: NCT01823861     History of Changes
Other Study ID Numbers: MarieStopes
First Submitted: March 30, 2013
First Posted: April 4, 2013
Last Update Posted: May 28, 2014
Last Verified: May 2014