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Mobile Technology for Improved Family Planning (MOTIF)

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.
 
ClinicalTrials.gov Identifier: NCT01823861
Recruitment Status : Completed
First Posted : April 4, 2013
Results First Posted : March 16, 2020
Last Update Posted : March 16, 2020
Sponsor:
Collaborator:
London School of Hygiene and Tropical Medicine
Information provided by (Responsible Party):
Marie Stopes International

Study Type Interventional
Study Design Allocation: Randomized;   Intervention Model: Parallel Assignment;   Masking: Single (Outcomes Assessor);   Primary Purpose: Supportive Care
Conditions Contraception
Post-abortion Family Planning
mHealth
Intervention Behavioral: Mobile phone-based intervention
Enrollment 500
Recruitment Details  
Pre-assignment Details  
Arm/Group Title Mobile Phone-based Intervention Standard Care
Hide Arm/Group Description

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.

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.

Face-to-face post-abortion family planning (PAFP) counselling, follow-up at one or two weeks, clinic phone number, existing 'Hotline' phone number.
Period Title: 4 Month Follow up
Started 249 251
Completed 211 220
Not Completed 38 31
Period Title: 12 Month Follow up
Started 211 220
Completed 169 159
Not Completed 42 61
Arm/Group Title Mobile Phone-based Intervention Standard Care Total
Hide Arm/Group Description

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.

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.

Face-to-face post-abortion family planning (PAFP) counselling, follow-up at one or two weeks, clinic phone number, existing 'Hotline' phone number. Total of all reporting groups
Overall Number of Baseline Participants 249 251 500
Hide Baseline Analysis Population Description
[Not Specified]
Age, Customized  
Measure Type: Count of Participants
Unit of measure:  Participants
Number Analyzed 249 participants 251 participants 500 participants
<25
88
  35.3%
69
  27.5%
157
  31.4%
≥25
161
  64.7%
182
  72.5%
343
  68.6%
Sex: Female, Male  
Measure Type: Count of Participants
Unit of measure:  Participants
Number Analyzed 249 participants 251 participants 500 participants
Female
249
 100.0%
251
 100.0%
500
 100.0%
Male
0
   0.0%
0
   0.0%
0
   0.0%
1.Primary Outcome
Title Use of a Effective Contraceptive Method at Four-months Post-abortion
Hide Description Self-reported use of pill, coil, implant or injection for all participants. Objective measurement of contraceptive use for participants from one clinic.
Time Frame 4 months
Hide Outcome Measure Data
Hide Analysis Population Description
[Not Specified]
Arm/Group Title Mobile Phone-based Intervention Standard Care
Hide Arm/Group Description:

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.

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.

Face-to-face post-abortion family planning (PAFP) counselling, follow-up at one or two weeks, clinic phone number, existing 'Hotline' phone number.
Overall Number of Participants Analyzed 211 220
Measure Type: Number
Unit of Measure: participants
135 101
2.Secondary Outcome
Title Pregnancy
Hide Description [Not Specified]
Time Frame 4 months
Outcome Measure Data Not Reported
3.Secondary Outcome
Title Repeat Abortion
Hide Description [Not Specified]
Time Frame 4 months
Outcome Measure Data Not Reported
4.Secondary Outcome
Title Contraceptive Discontinuation
Hide Description [Not Specified]
Time Frame 4 months
Outcome Measure Data Not Reported
Time Frame [Not Specified]
Adverse Event Reporting Description [Not Specified]
 
Arm/Group Title Mobile Phone-based Intervention Standard Care
Hide Arm/Group Description

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.

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.

Face-to-face post-abortion family planning (PAFP) counselling, follow-up at one or two weeks, clinic phone number, existing 'Hotline' phone number.
All-Cause Mortality
Mobile Phone-based Intervention Standard Care
Affected / at Risk (%) Affected / at Risk (%)
Total   --/--   --/-- 
Hide Serious Adverse Events
Mobile Phone-based Intervention Standard Care
Affected / at Risk (%) Affected / at Risk (%)
Total   0/249 (0.00%)   0/251 (0.00%) 
Hide Other (Not Including Serious) Adverse Events
Frequency Threshold for Reporting Other Adverse Events 0%
Mobile Phone-based Intervention Standard Care
Affected / at Risk (%) Affected / at Risk (%)
Total   0/249 (0.00%)   0/251 (0.00%) 
Certain Agreements
Principal Investigators are NOT employed by the organization sponsoring the study.
There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
Results Point of Contact
Layout table for Results Point of Contact information
Name/Title: Dr. Chris Smith
Organization: London School of Hygiene and Tropical Medicine
Phone: 07974562199
EMail: christopher.smith@lshtm.ac.uk
Layout table for additonal information
Responsible Party: Marie Stopes International
ClinicalTrials.gov Identifier: NCT01823861    
Other Study ID Numbers: MarieStopes
First Submitted: March 30, 2013
First Posted: April 4, 2013
Results First Submitted: March 2, 2020
Results First Posted: March 16, 2020
Last Update Posted: March 16, 2020