Trial Outcomes & Findings for Mobile Technology for Improved Family Planning (NCT NCT01823861)
NCT ID: NCT01823861
Last Updated: 2020-03-16
Results Overview
Self-reported use of pill, coil, implant or injection for all participants. Objective measurement of contraceptive use for participants from one clinic.
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
500 participants
Primary outcome timeframe
4 months
Results posted on
2020-03-16
Participant Flow
Participant milestones
| Measure |
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.
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.
|
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.
|
|---|---|---|
|
4 Month Follow up
STARTED
|
249
|
251
|
|
4 Month Follow up
COMPLETED
|
211
|
220
|
|
4 Month Follow up
NOT COMPLETED
|
38
|
31
|
|
12 Month Follow up
STARTED
|
211
|
220
|
|
12 Month Follow up
COMPLETED
|
169
|
159
|
|
12 Month Follow up
NOT COMPLETED
|
42
|
61
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Mobile Technology for Improved Family Planning
Baseline characteristics by cohort
| Measure |
Mobile Phone-based Intervention
n=249 Participants
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.
|
Standard Care
n=251 Participants
Face-to-face post-abortion family planning (PAFP) counselling, follow-up at one or two weeks, clinic phone number, existing 'Hotline' phone number.
|
Total
n=500 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Customized
<25
|
88 Participants
n=5 Participants
|
69 Participants
n=7 Participants
|
157 Participants
n=5 Participants
|
|
Age, Customized
≥25
|
161 Participants
n=5 Participants
|
182 Participants
n=7 Participants
|
343 Participants
n=5 Participants
|
|
Sex: Female, Male
Female
|
249 Participants
n=5 Participants
|
251 Participants
n=7 Participants
|
500 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=5 Participants
|
0 Participants
n=7 Participants
|
0 Participants
n=5 Participants
|
PRIMARY outcome
Timeframe: 4 monthsSelf-reported use of pill, coil, implant or injection for all participants. Objective measurement of contraceptive use for participants from one clinic.
Outcome measures
| Measure |
Mobile Phone-based Intervention
n=211 Participants
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.
|
Standard Care
n=220 Participants
Face-to-face post-abortion family planning (PAFP) counselling, follow-up at one or two weeks, clinic phone number, existing 'Hotline' phone number.
|
|---|---|---|
|
Use of a Effective Contraceptive Method at Four-months Post-abortion
|
135 participants
|
101 participants
|
SECONDARY outcome
Timeframe: 4 monthsOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 4 monthsOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 4 monthsOutcome measures
Outcome data not reported
Adverse Events
Mobile Phone-based Intervention
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Standard Care
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Dr. Chris Smith
London School of Hygiene and Tropical Medicine
Phone: 07974562199
Email: [email protected]
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place