Mobile Technology for Improved Family Planning (MOTIF)

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
London School of Hygiene and Tropical Medicine
Information provided by (Responsible Party):
Marie Stopes International
ClinicalTrials.gov Identifier:
NCT01823861
First received: March 30, 2013
Last updated: May 27, 2014
Last verified: May 2014
  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 Blind (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 ] [ Designated as safety issue: No ]
    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 ] [ Designated as safety issue: No ]
  • Repeat abortion [ Time Frame: 4 months ] [ Designated as safety issue: No ]
  • Contraceptive discontinuation [ Time Frame: 4 months ] [ Designated as safety issue: No ]

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

Ages Eligible for Study:   18 Years and older
Genders 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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01823861

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

No publications provided by Marie Stopes International

Additional 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
Study First Received: March 30, 2013
Last Updated: May 27, 2014
Health Authority: Cambodia: Ministry of Health

ClinicalTrials.gov processed this record on July 31, 2014