Trial Outcomes & Findings for The Effect of a Father Inclusive Psychoeducation Program on Postnatal Depression (NCT NCT02010840)
NCT ID: NCT02010840
Last Updated: 2025-10-29
Results Overview
Edinburgh Postnatal Depression Scale
Recruitment status
COMPLETED
Study phase
NA
Target enrollment
388 participants
Primary outcome timeframe
6 weeks postpartum
Results posted on
2025-10-29
Participant Flow
Participant milestones
| Measure |
Psychodeucation program
Both couples receive the father inclusive psychoeducation program which consists of a single 3-hour session during pregnancy and two telephone follow up at postpartum.
Psychoeducation program
|
Mother only
Only the women receives the psychoeducation program.
Psychoeducation program
|
Control group
Receives usual perinatal care services only
|
|---|---|---|---|
|
Overall Study
STARTED
|
134
|
124
|
130
|
|
Overall Study
COMPLETED
|
134
|
124
|
130
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
The Effect of a Father Inclusive Psychoeducation Program on Postnatal Depression
Baseline characteristics by cohort
| Measure |
Psychodeucation Program
n=134 Participants
Both couples receive the father inclusive psychoeducation program which consists of a single 3-hour session during pregnancy and two telephone follow up at postpartum.
Psychoeducation program
|
Mother Only
n=124 Participants
Only the women receives the psychoeducation program.
Psychoeducation program
|
Control Group
n=130 Participants
Receives usual perinatal care services only
|
Total
n=388 Participants
Total of all reporting groups
|
|---|---|---|---|---|
|
Age, Continuous
|
32 years
STANDARD_DEVIATION 4 • n=5 Participants
|
32 years
STANDARD_DEVIATION 4 • n=7 Participants
|
31 years
STANDARD_DEVIATION 4 • n=5 Participants
|
32 years
STANDARD_DEVIATION 4 • n=4 Participants
|
|
Sex: Female, Male
Female
|
67 Participants
n=5 Participants
|
62 Participants
n=7 Participants
|
65 Participants
n=5 Participants
|
194 Participants
n=4 Participants
|
|
Sex: Female, Male
Male
|
67 Participants
n=5 Participants
|
62 Participants
n=7 Participants
|
65 Participants
n=5 Participants
|
194 Participants
n=4 Participants
|
|
Race/Ethnicity, Customized
Chinese
|
134 Participants
n=5 Participants
|
124 Participants
n=7 Participants
|
130 Participants
n=5 Participants
|
388 Participants
n=4 Participants
|
PRIMARY outcome
Timeframe: 6 weeks postpartumEdinburgh Postnatal Depression Scale
Outcome measures
| Measure |
Psychodeucation program
n=134 Participants
Both couples receive the father inclusive psychoeducation program which consists of a single 3-hour session during pregnancy and two telephone follow up at postpartum.
Psychoeducation program
|
Mother only
n=124 Participants
Only the women receives the psychoeducation program.
Psychoeducation program
|
Control group
n=130 Participants
Receives usual perinatal care services only
|
|---|---|---|---|
|
Edinburgh Postnatal Depression Scale
|
41 score on a scale
Standard Error 0
|
35 score on a scale
Standard Error 0
|
37 score on a scale
Standard Error 0
|
SECONDARY outcome
Timeframe: 6 months postpartumOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 12 months postpartumOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 6 weeks postpartumOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 6 months postpartumOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 12 months postpartumOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 6 weeks postpartumOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 6 months postpartumOutcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 12 months postpartumOutcome measures
Outcome data not reported
Adverse Events
Psychodeucation program
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Mother only
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Control group
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
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place