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Social Media-Based Parenting Program for Women With Postpartum Depressive Symptoms

Social Media-Based Parenting Program for Women With Postpartum Depressive Symptoms

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04045132
Enrollment
75
Registered
2019-08-05
Start date
2019-12-17
Completion date
2021-10-07
Last updated
2023-12-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parent-Child Relations, Parenting, Postpartum Depression

Keywords

Social Media, Postpartum Depression, Parenting, Infants, Mothers

Brief summary

The purpose of this study is to determine whether a social media-based parenting program can improve responsive parenting among mothers with Postpartum depression (PPD) symptoms. Participants will be randomized to receive the parenting program plus online depression treatment or online depression treatment alone to assess target engagement. Our overall objective for this application is to study whether this program combined with online depression treatment leads to more responsive parenting (target) and signals improved child language, socioemotional and cognitive development (outcomes) compared to depression treatment alone.

Detailed description

Postpartum depression (PPD) symptoms are common among women following the birth of a child and can adversely impact a mother's ability to care for her child. As a result, infants of mothers with PPD symptoms may experience less responsive parenting, placing them at greater risk for delays in development. Evidence- based parenting programs have been developed to guide mothers with caring for their infants but may not address the impact of depression on parenting, are intensive and expensive to administer with limited ability for scale up, or are not available in a format that facilitates participation by women with depressive symptoms. To address these barriers, we developed a theoretically-driven social media-based parenting program on responsive parenting and child development. To determine whether the social media-based parenting program can improve responsive parenting among women with PPD symptoms, we will conduct a prospective individually randomized group treatment trial. 75 eligible women who screen positive for PPD at their infants' well child visit and their children will be consented, enrolled, and randomized as mother-child dyads 1:1 to receive a) the social media-based parenting program plus online depression treatment or b) online depression treatment alone. We chose a randomized design, because it is most effective in guarding against bias and will ensure that patients in both arms are similar in observed and unobserved characteristics. Treatment assignment will be done at the time of enrollment following informed consent. Descriptive statistics for demographic and poverty characteristics and PPD symptoms measured at baseline will be examined across the two treatment groups to assess the success of the randomization. We will assess responsive parenting at baseline and 3 months post-enrollment. Secondary outcomes, including changes in EPDS, BDI-II PSOC, and PSI-SF scores measured between baseline and the 3-month follow-up between groups, will be explored to determine if the effects of the parenting program are consistent with preliminary pilot findings. The intervention arm will also be assessed with the Therapeutic Factors Inventory-8 (TFI-8) to measure cohesion and the Acceptability survey which measures feasibility of the parenting program at 3-months post-enrollment. Additionally, at the 3-month mark, all participants will be administered the MoodGym Acceptability Survey to assess feasibility of the online depression treatment program. The results of this application would be expected to contribute important new knowledge and inform a future trial on parenting strategies to better assist mothers with PPD symptoms and improve child developmental outcomes.

Interventions

Participants in the intervention group will be enrolled in Facebook secret user groups, administered by a trained facilitator, in order to permit participants to view and comment on posted materials. Content and user identity are restricted to invited participants to maintain privacy. For each topic, we organize educational materials into video vignettes, narrated PowerPoint presentations, and written materials. The facilitator reviews and comments on postings daily, provides feedback to participants, and removes inappropriate postings if they occur. Facebook analytics for the secret groups are available to group administrators and will provide information on any sessions viewed (engagement) and counts of sessions viewed and comments posted (dosage). Women in the intervention group will also be enrolled in the online depression treatment program, MoodGym.

BEHAVIORALMoodGym

Participants in the control group will be enrolled in MoodGym, an evidence-based online Cognitive Behavioral Therapy (CBT) program for depression. Through the MoodGym program, participants will have access to interactive exercises, workbooks, anxiety and depression quizzes, and downloadable relaxation audio files. We will supplement Moodgym with a facilitator contact by texting or email to check-in and encourage completion of intervention. MoodGym will provide information on the number of sessions completed by participants (engagement and dosage).

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
Children's Hospital of Philadelphia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Video coders will be blinded to intervention assignment.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Women who: * Are \>18 years old * Screen positive for postpartum depression (score\>9) on the EPDS at a participating pediatric practice * Have an infant \<8 months of age * Speak and Read English * Have Access to a smart phone or computer tablet with internet access Children who: * Are \< 8 months old

Exclusion criteria

Women who: * Report suicidality (i.e., suicidal ideation and/or behavior) on the EPDS (Question #10) at enrollment. * Report severe depressive symptoms (EPDS\>20) at enrollment. * Have a substantiated report of child maltreatment Children who: * Were born premature (estimated gestational age\<35 weeks) * Have been diagnosed with congenital malformations or genetic syndromes which place them at risk of developmental delays * Are already currently receiving early intervention services for developmental delays at baseline

Design outcomes

Primary

MeasureTime frameDescription
The Parent Child Early Relational Assessment (PCERA)Baseline and 3 MonthsThe Parent Child Early Relational Assessment (PCERA) is a validated 65-item videotape assessment designed to measure the quality of affect and behavior in parent-infant interactions. The PCERA uses ratings that are based on observations of 5-minute videotaped interactions with parent-infant dyads engaged in free play. The PCERA has been shown to possess good interrater reliability, internal consistency, discriminant and concurrent validity, and sensitivity to change. The PCERA contains 8 subscales of which 3 parenting subscales will be the focus: 1) Parental Positive Affective Involvement and Verbalization, 2) Parental Negative Affect and Behavior, and 3) Parental Intrusiveness, Insensitivity, and Inconsistency. Each individual subscale is scored between 0-5, with higher scores indicating more responsive parenting. A subscale score of 1-2 indicates an area of concern, a score of 3 indicates some concern, and a score of 4-5 indicates an area of strength.

Secondary

MeasureTime frameDescription
The Beck Depression Inventory (BDI-II)Baseline and 3-monthsThe Beck Depression Inventory (BDI-II) is a 21-item self-report tool that measures the severity of depression and includes two subscales: cognitive and somatic. It has been well validated, and widely used, with scores 14-19 indicating mild depression, 20-28 moderate depression, and 29-63 severe depression. The total score (range: 0-63) will be used, with higher scores indicating higher levels of depression. These outcomes will assess changes in BDI-II from baseline to 3 months.
The Parenting Sense of Competence Scale (PSOC)Baseline and 3 monthsThe Parenting Sense of Competence Scale (PSOC) is a validated 17-item self-report measure of parenting self-esteem and competence and consists of two factors: satisfaction and efficacy. Response categories are on a 6-point likert-scale from strongly disagree to strongly agree. The total score (range: 17-102), which includes the sum of the two factors, will be used. A higher score indicates a higher parenting sense of competency. There are no average scores or 'cut-off's' for this tool. These outcomes will assess changes in PSOC from baseline to 3 months.
The Parenting Stress Index-Short Form (PSI-SF)Baseline and 3 monthsThe Parenting Stress Index-Short Form (PSI-SF) is a validated 36-item scale that measures parenting stress. The PSI-SF is a direct derivative of the full-length test (PSI) and it has been shown to have excellent internal consistency and to be positively associated with maternal psychological distress. Scores on the PSI-SF correlate well with the full-length PSI. It yields a Total Stress score from three scales: Parental Distress, Parent-Child Dysfunctional Interaction, and Difficult Child. The total score (range: 36-180) will be used, with higher scores indicating higher levels of stress.These outcomes will assess changes in PSI-SF from baseline to 3 months.
The National Comorbidity Survey (NCS)1-month, 2-month, 3-monthThe National Comorbidity Survey (NCS) provides data on mental health treatment in the United States. We will include a question from the NCS on prior mental health services use in the past month: In the past month, did you receive treatment for problems with your emotions or nerves, or your use of alcohol or drugs? We will consider mental health service use to have occurred in the past month if a mother responds Yes to this question. The results indicate the number of participants from each group who received mental health services/treatment at each time point. Additionally, if a mother responds Yes to the initial NCS item, a follow-up question will be asked to determine the specific types of services that were accessed: If yes, what type of treatment did you receive?
The Edinburgh Postnatal Depression Scale (EPDS)Baseline, 1-month, 2-month, 3-monthThe Edinburgh Postnatal Depression Scale (EPDS) is a validated 10-item self-report measure of depressive symptoms with strong evidence for reliability, validity, and utility in varying populations. It has been used extensively in mental health research and provides cutpoints to determine the severity of depressive symptoms. It includes a question on suicidal thoughts and wishes (#10) that will be used to monitor for suicidality. The total score (range: 0-30) will be used with scores of 10 or higher representing minor or moderate depression and scores of 20 or greater representing severe depression.These outcomes will assess changes in EPDS from baseline to 3 months.
Therapeutic Factors Inventory (TFI-8)3 monthsThe TFI-8 is a validated 8-item scale that is used to measure cohesion and is continuous process monitoring for therapy groups. Scores on the TFI-8 correlate well with the full TFI. The total score (range: 8-56) will be used, with higher scores indicating greater cohesion within the group. The TFI-8 will be administered at the 3-month visit to the intervention group, only.
Acceptability Survey3 monthsThe Acceptability survey is a 10-item scaled with 3 additional open ended questions that will be used to assess feasibility of the parenting program. The total score (range: 9-45) will be used and the open ended questions will be qualitatively analyzed to help inform the acceptability scores. Higher scores on the acceptability survey indicate greater satisfaction and feasibility of the parenting program. The acceptability survey will be administered at the 3-month visit to the intervention, only.
MoodGym Acceptability Survey3 monthsThe MoodGym Acceptability survey will be used to assess feasibility of the online depression treatment program, MoodGym. The survey includes two qualitative open-ended questions and an additional question that asks, It is \_\_\_\_\_\_\_\_\_\_\_ that I will use MoodGym compared to going to a health care provider for depression treatment. The response is a 5-point likert-scale from Much More Likely to Much Less Likely. The open ended questions will be qualitatively analyzed to help inform the acceptability scores. The MoodGym Acceptability survey will be administered at the 3-month visit to both the intervention and control group.
Multi-dimensional Scale of Perceived Social Support (MSPSS)BaselineThe Multi-dimensional Scale of Perceived Social Support (MSPSS) is a 12-item scale that assesses perceived social support from family, friends, and a significant other. Response categories are on a 7-point likert-scale from 1=very strongly disagree to 7=very strongly agree. The total score will be used (range: 12-84).

Countries

United States

Participant flow

Recruitment details

From December 2019 to March 2020, recruitment took place over the phone and enrollment was completed on site at the Roberts Center for Pediatric Research at the Children's Hospital of Philadelphia. Due to the COVID-19 pandemic, there was a recruitment pause from March-June 2020. As of June 12th, 2020, the study was approved by the IRB to enroll participants to the study virtually, and remaining recruitment and enrollment activities were completed virtually.

Pre-assignment details

If a participant was enrolled to the study but did not complete the videotaped baseline Parent Child Early Relational Assessment before the start of the intervention, regardless of the group they were randomized to, they were withdrawn from the study.

Participants by arm

ArmCount
MoodGym Alone (Control)
The MoodGym program is an evidence-based online cognitive behavioral treatment program that has been shown to be effective at reducing depression symptoms in a meta-analysis of 11 trials (g=0.36, 95% CI 0.17-0.56). Moodgym contains five modules with interactive exercises, workbooks, anxiety and depression quizzes, and downloadable relaxation audio files that can be completed online without therapist interaction. MoodGym: Participants in the control group will be enrolled in MoodGym, an evidence-based online Cognitive Behavioral Therapy (CBT) program for depression. Through the MoodGym program, participants will have access to interactive exercises, workbooks, anxiety and depression quizzes, and downloadable relaxation audio files. We will supplement Moodgym with a facilitator contact by texting or email to check-in and encourage completion of intervention. MoodGym will provide information on the number of sessions completed by participants (engagement and dosage).
37
Parenting Program + MoodGym (Intervention)
The social media-based parenting program consists of 8 weekly sessions with the following topics: depression psychoeducation and behavioral activation, infant temperament, play, feeding, safety, sleep, parent-child interactions, and shared book reading. Participants in the experimental arm will also be enrolled in the online depression treatment program, MoodGym. Social Media-Based Parenting Program: Participants in the intervention group will be enrolled in Facebook secret user groups. Content and user identity are restricted to invited participants to maintain privacy. For each topic, we organize educational materials into video vignettes and written materials. The facilitator reviews and comments on postings daily, provides feedback to participants, and removes inappropriate postings if they occur. Facebook analytics for the secret groups are available to group administrators and will provide information on any sessions viewed (engagement) and counts of sessions viewed and comments posted (dosage). MoodGym: Participants in the control and intervention groups will be enrolled in MoodGym, an evidence-based online Cognitive Behavioral Therapy (CBT) program for depression. Through the MoodGym program, participants will have access to interactive exercises, workbooks, anxiety and depression quizzes, and downloadable relaxation audio files. We will supplement Moodgym with a facilitator contact by texting or email to check-in and encourage completion of intervention.
38
Total75

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up36

Baseline characteristics

CharacteristicMoodGym Alone (Control)TotalParenting Program + MoodGym (Intervention)
Age, Continuous28.5 years
STANDARD_DEVIATION 4.8
29.2 years
STANDARD_DEVIATION 5.2
29.8 years
STANDARD_DEVIATION 5.6
Ethnicity (NIH/OMB)
Hispanic or Latino
1 Participants3 Participants2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
36 Participants72 Participants36 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
>1 Race/Other
1 participants4 participants3 participants
Race/Ethnicity, Customized
American Indian/Alaska Native
0 participants0 participants0 participants
Race/Ethnicity, Customized
Asian
0 participants0 participants0 participants
Race/Ethnicity, Customized
Black
28 participants52 participants24 participants
Race/Ethnicity, Customized
Native Hawaiian or Other Pacific Islander
1 participants1 participants0 participants
Race/Ethnicity, Customized
White
7 participants18 participants11 participants
Region of Enrollment
United States
37 participants75 participants38 participants
Sex: Female, Male
Female
37 Participants75 Participants38 Participants
Sex: Female, Male
Male
0 Participants0 Participants0 Participants
The Parent Child Early Relational Assessment (PCERA)
PCERA Factor 1 (Baseline)- Parental Positive Affective Involvement and Verbalization
3.0 score on a scale
STANDARD_DEVIATION 0.6
3.1 score on a scale
STANDARD_DEVIATION 0.6
3.2 score on a scale
STANDARD_DEVIATION 0.6
The Parent Child Early Relational Assessment (PCERA)
PCERA Factor 2 (Baseline)- Parental Negative Affect and Behavior
4.1 score on a scale
STANDARD_DEVIATION 0.7
4.1 score on a scale
STANDARD_DEVIATION 0.8
4.0 score on a scale
STANDARD_DEVIATION 0.8
The Parent Child Early Relational Assessment (PCERA)
PCERA Factor 3 (Baseline)- Parental Intrusiveness, Insensitivity, and Inconsistency
3.1 score on a scale
STANDARD_DEVIATION 0.4
3.1 score on a scale
STANDARD_DEVIATION 0.6
3.1 score on a scale
STANDARD_DEVIATION 0.7

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 370 / 38
other
Total, other adverse events
7 / 378 / 38
serious
Total, serious adverse events
2 / 372 / 37

Outcome results

Primary

The Parent Child Early Relational Assessment (PCERA)

The Parent Child Early Relational Assessment (PCERA) is a validated 65-item videotape assessment designed to measure the quality of affect and behavior in parent-infant interactions. The PCERA uses ratings that are based on observations of 5-minute videotaped interactions with parent-infant dyads engaged in free play. The PCERA has been shown to possess good interrater reliability, internal consistency, discriminant and concurrent validity, and sensitivity to change. The PCERA contains 8 subscales of which 3 parenting subscales will be the focus: 1) Parental Positive Affective Involvement and Verbalization, 2) Parental Negative Affect and Behavior, and 3) Parental Intrusiveness, Insensitivity, and Inconsistency. Each individual subscale is scored between 0-5, with higher scores indicating more responsive parenting. A subscale score of 1-2 indicates an area of concern, a score of 3 indicates some concern, and a score of 4-5 indicates an area of strength.

Time frame: Baseline and 3 Months

Population: Participants who completed both a Baseline and 3-month follow-up Parent Child Early Relational Assessment (PCERA) videotape measure were included in the overall analysis. At Baseline, 73 (36 control and 37 intervention) of the 75 total enrolled participants completed a PCERA videotape measure, and 66 (34 control and 32 intervention) of the 75 total enrolled participants completed a PCERA videotape measure at 3-month follow-up.

ArmMeasureGroupValue (MEAN)Dispersion
MoodGym Alone (Control)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 1 (Baseline)- Parental Positive Affective Involvement and Verbalization3.0 score on a scaleStandard Deviation 0.6
MoodGym Alone (Control)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 1 (3-month follow-up)- Parental Positive Affective Involvement and Verbalization3.3 score on a scaleStandard Deviation 0.5
MoodGym Alone (Control)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 2 (Baseline)- Parental Negative Affect and Behavior4.1 score on a scaleStandard Deviation 0.7
MoodGym Alone (Control)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 2 (3-month follow-up)- Parental Negative Affect and Behavior4.3 score on a scaleStandard Deviation 0.6
MoodGym Alone (Control)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 3 (Baseline)- Parental Intrusiveness, Insensitivity, and Inconsistency3.1 score on a scaleStandard Deviation 0.4
MoodGym Alone (Control)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 3 (3-month follow-up)- Parental Intrusiveness, Insensitivity, and Inconsistency3.5 score on a scaleStandard Deviation 0.5
Parenting Program + MoodGym (Intervention)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 3 (Baseline)- Parental Intrusiveness, Insensitivity, and Inconsistency3.1 score on a scaleStandard Deviation 0.7
Parenting Program + MoodGym (Intervention)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 1 (Baseline)- Parental Positive Affective Involvement and Verbalization3.2 score on a scaleStandard Deviation 0.6
Parenting Program + MoodGym (Intervention)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 2 (3-month follow-up)- Parental Negative Affect and Behavior4.2 score on a scaleStandard Deviation 0.8
Parenting Program + MoodGym (Intervention)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 1 (3-month follow-up)- Parental Positive Affective Involvement and Verbalization3.3 score on a scaleStandard Deviation 0.6
Parenting Program + MoodGym (Intervention)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 3 (3-month follow-up)- Parental Intrusiveness, Insensitivity, and Inconsistency3.4 score on a scaleStandard Deviation 0.6
Parenting Program + MoodGym (Intervention)The Parent Child Early Relational Assessment (PCERA)PCERA Factor 2 (Baseline)- Parental Negative Affect and Behavior4.0 score on a scaleStandard Deviation 0.8
Secondary

Acceptability Survey

The Acceptability survey is a 10-item scaled with 3 additional open ended questions that will be used to assess feasibility of the parenting program. The total score (range: 9-45) will be used and the open ended questions will be qualitatively analyzed to help inform the acceptability scores. Higher scores on the acceptability survey indicate greater satisfaction and feasibility of the parenting program. The acceptability survey will be administered at the 3-month visit to the intervention, only.

Time frame: 3 months

Population: Participants in the Parenting Program + MoodGym (Intervention arm), only. At the 3-month time point, there were several participants who had been lost to follow-up and did not complete the Acceptability Survey measure. This is the reason for the drop in number of participants.

ArmMeasureValue (MEAN)
Parenting Program + MoodGym (Intervention)Acceptability Survey34.8 score on a scale
Secondary

MoodGym Acceptability Survey

The MoodGym Acceptability survey will be used to assess feasibility of the online depression treatment program, MoodGym. The survey includes two qualitative open-ended questions and an additional question that asks, It is \_\_\_\_\_\_\_\_\_\_\_ that I will use MoodGym compared to going to a health care provider for depression treatment. The response is a 5-point likert-scale from Much More Likely to Much Less Likely. The open ended questions will be qualitatively analyzed to help inform the acceptability scores. The MoodGym Acceptability survey will be administered at the 3-month visit to both the intervention and control group.

Time frame: 3 months

Population: Participants who completed a 3-month MoodGym Acceptability Survey measure were included in the overall analysis. At the 3-month time point, there were several participants who had been lost to follow-up and did not complete the MoodGym Acceptability Survey measure. This is the reason for the drop in number of participants.

ArmMeasureCategoryValue (COUNT_OF_PARTICIPANTS)
MoodGym Alone (Control)MoodGym Acceptability SurveyMuch More Likely7 Participants
MoodGym Alone (Control)MoodGym Acceptability SurveyLess Likely3 Participants
MoodGym Alone (Control)MoodGym Acceptability SurveyMore Likely9 Participants
MoodGym Alone (Control)MoodGym Acceptability SurveyMuch Less Likely6 Participants
MoodGym Alone (Control)MoodGym Acceptability SurveyNo Difference7 Participants
Parenting Program + MoodGym (Intervention)MoodGym Acceptability SurveyMuch Less Likely4 Participants
Parenting Program + MoodGym (Intervention)MoodGym Acceptability SurveyMuch More Likely6 Participants
Parenting Program + MoodGym (Intervention)MoodGym Acceptability SurveyNo Difference11 Participants
Parenting Program + MoodGym (Intervention)MoodGym Acceptability SurveyLess Likely4 Participants
Parenting Program + MoodGym (Intervention)MoodGym Acceptability SurveyMore Likely6 Participants
Secondary

Multi-dimensional Scale of Perceived Social Support (MSPSS)

The Multi-dimensional Scale of Perceived Social Support (MSPSS) is a 12-item scale that assesses perceived social support from family, friends, and a significant other. Response categories are on a 7-point likert-scale from 1=very strongly disagree to 7=very strongly agree. The total score will be used (range: 12-84).

Time frame: Baseline

Population: Participants who completed a Baseline Multi-dimensional Scale of Perceived Social Support (MSPSS) measure were included in the overall analysis. At Baseline, 74 (37 control and 37 intervention) of the 75 total enrolled participants completed the MSPSS measure.

ArmMeasureValue (MEAN)
MoodGym Alone (Control)Multi-dimensional Scale of Perceived Social Support (MSPSS)52.9 score on a scale
Parenting Program + MoodGym (Intervention)Multi-dimensional Scale of Perceived Social Support (MSPSS)58.0 score on a scale
Secondary

The Beck Depression Inventory (BDI-II)

The Beck Depression Inventory (BDI-II) is a 21-item self-report tool that measures the severity of depression and includes two subscales: cognitive and somatic. It has been well validated, and widely used, with scores 14-19 indicating mild depression, 20-28 moderate depression, and 29-63 severe depression. The total score (range: 0-63) will be used, with higher scores indicating higher levels of depression. These outcomes will assess changes in BDI-II from baseline to 3 months.

Time frame: Baseline and 3-months

Population: Participants who completed the Beck Depression Inventory (BDI-II) measure at each time point were included in the analysis. At baseline there was one participant, of the 75 total enrolled, who did not complete any baseline measures, including the BDI-II. Over the 3-month time frame there were several participants who were lost to follow-up and did not complete the BDI-II measure. This is the reason for the drop in number of participants analyzed between groups over the 3-month period.

ArmMeasureGroupValue (MEAN)
MoodGym Alone (Control)The Beck Depression Inventory (BDI-II)BDI-II Baseline23.6 score on a scale
MoodGym Alone (Control)The Beck Depression Inventory (BDI-II)BDI-II 3-month follow-up14.6 score on a scale
Parenting Program + MoodGym (Intervention)The Beck Depression Inventory (BDI-II)BDI-II Baseline22.4 score on a scale
Parenting Program + MoodGym (Intervention)The Beck Depression Inventory (BDI-II)BDI-II 3-month follow-up14.3 score on a scale
Secondary

The Edinburgh Postnatal Depression Scale (EPDS)

The Edinburgh Postnatal Depression Scale (EPDS) is a validated 10-item self-report measure of depressive symptoms with strong evidence for reliability, validity, and utility in varying populations. It has been used extensively in mental health research and provides cutpoints to determine the severity of depressive symptoms. It includes a question on suicidal thoughts and wishes (#10) that will be used to monitor for suicidality. The total score (range: 0-30) will be used with scores of 10 or higher representing minor or moderate depression and scores of 20 or greater representing severe depression.These outcomes will assess changes in EPDS from baseline to 3 months.

Time frame: Baseline, 1-month, 2-month, 3-month

Population: Participants who completed the Edinburgh Postnatal Depression Scale (EPDS) measure at each time point were included in the analysis. Over the 3-month time frame there were several participants who were lost to follow-up and did not complete the subsequent EPDS measures. This is the reason for the drop in number of participants analyzed between groups over the 3-month period.

ArmMeasureGroupValue (MEAN)
MoodGym Alone (Control)The Edinburgh Postnatal Depression Scale (EPDS)EPDS Baseline15.2 score on a scale
MoodGym Alone (Control)The Edinburgh Postnatal Depression Scale (EPDS)EPDS 1-month follow-up12.6 score on a scale
MoodGym Alone (Control)The Edinburgh Postnatal Depression Scale (EPDS)EPDS 2-month follow-up11.7 score on a scale
MoodGym Alone (Control)The Edinburgh Postnatal Depression Scale (EPDS)EPDS 3-month follow-up10.1 score on a scale
Parenting Program + MoodGym (Intervention)The Edinburgh Postnatal Depression Scale (EPDS)EPDS 3-month follow-up9.0 score on a scale
Parenting Program + MoodGym (Intervention)The Edinburgh Postnatal Depression Scale (EPDS)EPDS Baseline14.3 score on a scale
Parenting Program + MoodGym (Intervention)The Edinburgh Postnatal Depression Scale (EPDS)EPDS 2-month follow-up9.7 score on a scale
Parenting Program + MoodGym (Intervention)The Edinburgh Postnatal Depression Scale (EPDS)EPDS 1-month follow-up9.7 score on a scale
Secondary

The National Comorbidity Survey (NCS)

The National Comorbidity Survey (NCS) provides data on mental health treatment in the United States. We will include a question from the NCS on prior mental health services use in the past month: In the past month, did you receive treatment for problems with your emotions or nerves, or your use of alcohol or drugs? We will consider mental health service use to have occurred in the past month if a mother responds Yes to this question. The results indicate the number of participants from each group who received mental health services/treatment at each time point. Additionally, if a mother responds Yes to the initial NCS item, a follow-up question will be asked to determine the specific types of services that were accessed: If yes, what type of treatment did you receive?

Time frame: 1-month, 2-month, 3-month

Population: Participants who completed the National Comorbidity Survey (NCS) measure at each time point were included in the analysis. Over the 3-month time frame there were several participants who were lost to follow-up and did not complete the NCSmeasure. This is the reason for the drop in number of participants analyzed between groups over the 3-month period.

ArmMeasureGroupValue (COUNT_OF_PARTICIPANTS)
MoodGym Alone (Control)The National Comorbidity Survey (NCS)NCS 1-month follow-up10 Participants
MoodGym Alone (Control)The National Comorbidity Survey (NCS)NCS 2-month follow-up12 Participants
MoodGym Alone (Control)The National Comorbidity Survey (NCS)NCS 3-month follow-up11 Participants
Parenting Program + MoodGym (Intervention)The National Comorbidity Survey (NCS)NCS 1-month follow-up7 Participants
Parenting Program + MoodGym (Intervention)The National Comorbidity Survey (NCS)NCS 2-month follow-up8 Participants
Parenting Program + MoodGym (Intervention)The National Comorbidity Survey (NCS)NCS 3-month follow-up10 Participants
Secondary

The Parenting Sense of Competence Scale (PSOC)

The Parenting Sense of Competence Scale (PSOC) is a validated 17-item self-report measure of parenting self-esteem and competence and consists of two factors: satisfaction and efficacy. Response categories are on a 6-point likert-scale from strongly disagree to strongly agree. The total score (range: 17-102), which includes the sum of the two factors, will be used. A higher score indicates a higher parenting sense of competency. There are no average scores or 'cut-off's' for this tool. These outcomes will assess changes in PSOC from baseline to 3 months.

Time frame: Baseline and 3 months

Population: Participants who completed the Parenting Sense of Competence Scale (PSOC) measure at each time point were included in the analysis. At baseline there was one participant, of the 75 total enrolled, who did not complete any baseline measures, including the PSOC. Over the 3-month time frame there were several participants who were lost to follow-up and did not complete the PSOC measure. This is the reason for the drop in number of participants analyzed between groups over the 3-month period.

ArmMeasureGroupValue (MEAN)
MoodGym Alone (Control)The Parenting Sense of Competence Scale (PSOC)PSOC Baseline63.2 score on a scale
MoodGym Alone (Control)The Parenting Sense of Competence Scale (PSOC)PSOC 3-month follow-up71.3 score on a scale
Parenting Program + MoodGym (Intervention)The Parenting Sense of Competence Scale (PSOC)PSOC Baseline63.9 score on a scale
Parenting Program + MoodGym (Intervention)The Parenting Sense of Competence Scale (PSOC)PSOC 3-month follow-up71.1 score on a scale
Secondary

The Parenting Stress Index-Short Form (PSI-SF)

The Parenting Stress Index-Short Form (PSI-SF) is a validated 36-item scale that measures parenting stress. The PSI-SF is a direct derivative of the full-length test (PSI) and it has been shown to have excellent internal consistency and to be positively associated with maternal psychological distress. Scores on the PSI-SF correlate well with the full-length PSI. It yields a Total Stress score from three scales: Parental Distress, Parent-Child Dysfunctional Interaction, and Difficult Child. The total score (range: 36-180) will be used, with higher scores indicating higher levels of stress.These outcomes will assess changes in PSI-SF from baseline to 3 months.

Time frame: Baseline and 3 months

Population: Participants who completed the Parenting Stress Index-Short Form (PSI-SF) measure at each time point were included in the analysis. At baseline there was one participant, of the 75 total enrolled, who did not complete any baseline measures, including the PSI-SF. Over the 3-month time frame there were several participants who were lost to follow-up and did not complete the PSI-SF measure. This is the reason for the drop in number of participants analyzed between groups over the 3-month period.

ArmMeasureGroupValue (MEAN)
MoodGym Alone (Control)The Parenting Stress Index-Short Form (PSI-SF)PSI-SF Baseline89.2 score on a scale
MoodGym Alone (Control)The Parenting Stress Index-Short Form (PSI-SF)PSI-SF 3-month follow-up75.5 score on a scale
Parenting Program + MoodGym (Intervention)The Parenting Stress Index-Short Form (PSI-SF)PSI-SF Baseline85.4 score on a scale
Parenting Program + MoodGym (Intervention)The Parenting Stress Index-Short Form (PSI-SF)PSI-SF 3-month follow-up73.6 score on a scale
Secondary

Therapeutic Factors Inventory (TFI-8)

The TFI-8 is a validated 8-item scale that is used to measure cohesion and is continuous process monitoring for therapy groups. Scores on the TFI-8 correlate well with the full TFI. The total score (range: 8-56) will be used, with higher scores indicating greater cohesion within the group. The TFI-8 will be administered at the 3-month visit to the intervention group, only.

Time frame: 3 months

Population: Participants in the Parenting Program + MoodGym (Intervention arm), only. At the 3-month time point, there were several participants who had been lost to follow-up and did not complete the TFI-8 measure. This is the reason for the drop in number of participants.

ArmMeasureValue (MEAN)
Parenting Program + MoodGym (Intervention)Therapeutic Factors Inventory (TFI-8)40.5 score on a scale

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026