| Literature DB >> 33096738 |
Aliyah Dosani1,2,3, Harshmeet Arora4, Sahil Mazmudar4.
Abstract
Women in low- and middle-income countries have high rates of perinatal depression. As smartphones become increasingly accessible around the world, there is an opportunity to explore innovative mHealth tools for the prevention, screening, and management of perinatal depression. We completed a scoping review of the literature pertaining to the use of mobile phone technologies for perinatal depression in low-and middle-income countries. PubMed CINHAL, and Google Scholar databases were searched, generating 423 results. 12 articles met our inclusion criteria. Two of the 12 articles reviewed mobile phone applications. The remaining 9 articles were study protocols or descriptive/intervention studies. Our results reveal that minimal literature is currently available on the use of mobile health for perinatal depression in low- and middle-income countries. We found four articles that present the results of an intervention that were delivered through mobile phones for the treatment of perinatal depressive symptoms and an additional qualitative study describing the perceptions of mothers receiving cognitive behavioral therapy via telephones. These studies demonstrated that depressive symptoms improved after the interventions. There is potential to improve the quality of mHealth interventions, specifically mobile phone applications for perinatal depressive symptoms and depression, through meaningful collaborative work between healthcare professionals and application developers.Entities:
Keywords: antenatal depression; low- and middle-income countries; mhealth; mobile phone health applications; perinatal depression; postpartum depression; resource-poor countries
Mesh:
Year: 2020 PMID: 33096738 PMCID: PMC7589927 DOI: 10.3390/ijerph17207679
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Figure 1Stages of the scoping literature review.
Search strategy.
| Category | Search Parameters |
|---|---|
| Population | (“Pregnancy”[Mesh] OR “pregnancy”[tw] OR “pregnancies”[tw] OR “pregnant”[tw] OR “Postpartum period”[Mesh] OR “postpartum”[tw] OR “post-partum”[tw] OR “post partum”[tw] OR “puerperium”[Mesh] OR “puerperium”[tw] OR “Perinatal care”[Mesh] OR “perinat*”[tw] OR “postnat*”[tw] OR “maternal”[tw] OR “Prenatal Care”[Mesh] OR “prenatal”[tw] OR “Prenatal education”[Mesh] OR “antenatal” OR “Puerperal Disorders”[Mesh]) AND |
| Intervention | (“mobile health”[tw] OR “mhealth”[tw] OR “ehealth”[tw] OR “m-health”[tw] OR “e-health”[tw] OR “mcare”[tw] OR “Cell Phones”[Mesh] OR “Computers, Handheld”[Mesh] OR “cell phones”[tw] OR “cell phone”[TW] OR “cellular phone”[tw] OR “cellular phones”[tw] OR “cellular telephone”[tw] OR “cellular telephones”[tw] OR “mobile phone”[tw] OR “mobile phones”[tw] OR “mobile telephone”[tw] OR “mobile telephones”[tw] OR “iphone”[tw] OR “ipad”[tw] OR “cellphone”[tw] OR “cellphones”[tw] OR “pda”[tw] OR “personal digital assistant”[tw] OR “blackberry”[tw] OR “android”[tw] OR “smartphone”[tw] OR “smartphones”[tw] OR “smart phone”[tw] OR “smart phones”[tw] OR “tablet”[tw] OR “handheld computer”[tw] OR “apps”[tw] OR “mobile application”[tw] OR “mobile applications”[tw] OR “mobile communication”[tw] OR “mobile technology”[tw] OR “mobile games”[tw]) AND |
| Outcome | (“depression”[Mesh] OR “depression”[TW] OR “depressed”[TW] OR “depression, postpartum”[Mesh] OR “mental health”[Mesh] OR “mental health”[TW] OR “Mental disorders”[Mesh] OR “mental disorder”[TW] OR anxiety[TW] OR “Anxiety Disorders”[Mesh] OR “Anxiety”[Mesh]) |
Data extraction: study design, study population, and details of the intervention.
| First Author, Year, Country | Study Design | Number of Participants ( | Study Population/Data Collection | Identification of Depressive Symptoms and Cut-Off Scores | Depression Assessment Time Points |
|---|---|---|---|---|---|
| Chan et al., 2019 [ | Single-blind randomized control trial | All first-time expectant mothers. | Validated Chinese version of the Edinburgh Postnatal Depression Scale (EPDS). No cut-off scores were provided. | First visit to antenatal clinic and follow-up at 4 weeks postpartum | |
| Green et al., 2019 [ | Single-case experimental design and qualitative interviews | Sample size has not been reported. | At least 20 weeks’ gestation or no more than 6 months postpartum. | Patient Health Questionnaire-9 (PHQ-9), and a question about mood on a 10-point scale. | Participants are randomized to a 1- or 2-week baseline period and then invited to begin using Zuri. Participants are prompted to rate their mood via SMS every 3 days during the baseline and intervention periods. |
| Gureje et al., 2015 [ | Randomized control trial | Pregnant women between the ages of 16 and 45 years. | -EPDS score ≥ 12 | Assessments will be undertaken at baseline, 2 months following recruitment into the study, and 3, 6, 9, and 12 months after childbirth. | |
| Jannati et al., 2020 [ | Non-blinded parallel-group randomized controlled trial | Women aged 18 or above. | EPDS score ≥13 Confirmed diagnosis of postpartum depression within two weeks after the participants’ recruitment using the International Neuropsychiatric Interview (MINI) | Assessments were undertaken at baseline and 2 months after baseline. | |
| Li et al., 2020 [ | Analyzed and evaluated the contents of all postpartum depression applications (iOS and Android) in China | 2 commentators used the PPD -related keywords to search for three application platforms in the Chinese market: Android, iOS, and WeChat, simplified Chinese and English. | Not applicable | Not applicable | |
| Mo et al., 2018 [ | Cross-sectional study | Pregnant women who attended Hunan Provincial Maternal and Child Health Hospital. | EPDS score ≥10 | One questionnaire was completed upon recruitment into the study | |
| Ngai et al., 2019 [ | Qualitative study with semi-structured interviews analyzed by content analysis. | A sample of 39 women from 197 was invited for semi-structured telephone interviews at 6 weeks postpartum. | EPDS score ≥10 | Not applicable | |
| Niksalehi et al., 2018 [ | Single-group, pre-test, and post-test study design. | -Healthy first-time mothers recruited from a medical university-affiliated hospital in Bandar Abbas city, Iran. | EPDS score ≥12 | Data were collected at baseline (14 days after giving birth) one week after receiving the intervention for 35 days. | |
| de Figueiredo et al., 2015 [ | Cross-sectional study | Pregnant women from 25 to 28 weeks of gestational age. | Edinburgh Postnatal Depression Scale (EPDS score ≥10) | During the first year after childbirth, the women enrolled in the original study were contacted by telephone and invited to answer the EPDS. | |
| Shamshiri Milani et al., 2015 [ | Randomized control trial | Postpartum women who had term deliveries, live births were uncomplicated deliveries. | Edinburgh Postnatal Depression Scale (EPDS score ≥ 10) | 10–15 days after childbirth and 6 weeks postpartum | |
| Sun et al., 2019 [ | Study protocol for a double-blind randomized controlled trial | Postpartum women up to 6 weeks post-delivery with EPDS score ≥9–≤12, selected randomly from one health left in each district within Changsha city. | Edinburgh Postnatal Depression Scale (EPDS score ≥9) | Baseline (t0), immediately after the last intervention (t1), 3 months following the intervention (t2), and 6 months following the intervention (t3). | |
| Zhang et al., 2017 [ | Evaluation of mobile phone applications to determine the quality of information presented for postnatal depression. | Apple iTunes and Google Android Play store applications searched. | Not applicable | Not applicable |
Data extraction: outcomes.
| First Author, Year | Intervention and Comparator Group | Primary Outcome Measure | Other Outcome Measures |
|---|---|---|---|
| Chan et al., 2019 [ | A mobile phone application called iParent, in addition to in-person nurse-led antenatal classes. | The difference in the levels of antenatal and postnatal depression | Differences between anxiety levels, stress levels, and health-related quality of life before and after the RCT. Anxiety and stress levels were assessed with the Anxiety and Stress subscales of the Depression Anxiety Stress Scale (DASS). Health-related QoL was measured by the 12-item Short-Form Health Survey (SF-12). |
| Green et al., 2019 [ | Automated the Thinking Healthy program via a mobile phone app called Healthy Moms over 15 sessions. | Depression severity and mood | Participant engagement with the mobile phone application, intervention feasibility, and acceptability, variability in patient response to treatment. |
| Gureje et al., 2015 [ | Intervention uses the WHO Mental Health Gap Action Programme Intervention Guide (mhGAP-IG) as adapted for the health system of Nigeria. | The primary outcome is recovery from depression (EPDS < 6) at 6 months | Disability as measured by the WHO and the Disability Assessment Scale. |
| Jannati et al., 2020 [ | Mobile phone-based cognitive-behavioral therapy (CBT) on postpartum depression called Happy Mom, with eight weekly lessons. | EPDS score post-intervention | None |
| Li et al., 2020 [ | Currently available Chinese mobile phone applications for postpartum depression. | The adherence of mobile phone applications with clinical practice-based guidelines. | The Mobile App Rating Scale (MARS) to evaluate engagement, functionality, aesthetics of the application features. |
| Mo et al., 2018 [ | No intervention as this was a descriptive study. | Use of antenatal care mobile phone applications and antenatal depression. | None |
| Ngai et al., 2019 [ | No interventions as this was a qualitative study. | Specific components of the T-CBT intervention that women considered helpful in their preparation for early motherhood. | Not applicable |
| Niksalehi et al., 2018 [ | Mobile phone SMS support for mothers with postpartum depression. | Depressive symptoms measured by the EDPS. | The satisfaction level of participants with the support received. |
| de Figueiredo et al., 2015 [ | EPDS administered | The reliability and validity of the EPDS were administered by telephone interviews. | None |
| Shamshiri Milani et al., 2015 [ | The intervention group received telephone support provided by eight healthy volunteers who were trained to communicate effectively with mothers to manage their problems. | EPDS score post-intervention | None |
| Sun et al., 2019 [ | Six CBT modules were delivered via mobile phone application to participants over six weeks. | Postpartum depression | Negative emotion symptoms measured by the depression, anxiety, and Stress Scale (DASS-21) |
| Zhang et al., 2017 [ | Silberg Scale was used in the assessment of the information quality of smartphone applications. | Information quality score of mobile applications | None |
Data extraction: results and limitations.
| First Author, Year | Attrition and Adherence | Results (Key Findings) | Limitations |
|---|---|---|---|
| Chan et al., 2019 [ | At the follow-up T2 survey after the intervention, the retention rates were 66.1% (n = 218) for the intervention group and 68.2% (n = 225) for the control group. | Associations found between: | The short postpartum period after which the follow-up assessment was conducted and the inclusion of first-time mothers rather than all mothers. |
| Green et al., 2019 [ | Not applicable | Study protocol—no results were reported. | Recruited women who live in urban and peri-urban lefts in one part of Kenya, thus forgoing generalization of the broader population of Kenyan women. |
| Gureje et al., 2015 [ | Not applicable | Study protocol - no results were reported. | None reported |
| Jannati et al., 2020 [ | No information provided | Before the intervention, there was no statistically significant difference between the EPDS score between the two groups ( | The small sample size necessitates replication. |
| Li et al., 2020 [ | Not applicable | Postpartum depression applications in China lack known effective intervention content. | There are no recent guidelines for the prevention of postpartum depression in China (latest in 2014) |
| Mo et al., 2018 [ | Not applicable | 71.31% (930/1304) of the pregnant women used mobile phone applications for antenatal care. | A cross-sectional study design led to limited data extrapolation, lacking causal inference. |
| Ngai et al., 2019 [ | None | Majority of mothers | The results of this study may not be generalizable due to the small sample size. |
| Niksalehi et al., 2018 [ | 56 women were initially enrolled and n = 2 were lost | Mean score of EDPS pre-intervention was 14.44 (SD = 2.66). | The single-group and pre–post-study design that may have resulted in Selection bias resulting in a homogenous sample that limits the generalizability of the results. |
| de Figueiredo et al., 2015 [ | 161 mothers who had EPDS ≥ 10 withdrew from the study | In 90 participants, the diagnosis of the major depressive episode was confirmed by the diagnostic interview (EPDS ≥10 = 65; EPDS ˂10 = 23). | The large number of subjects who did not attend the diagnostic assessment (61.3%) despite multiple attempts to schedule the face-to-face interviews. |
| Shamshiri Milani et al., 2015 [ | There were 5 participants from the intervention group and 3 from the control group that were lost to follow up. Therefore n = 46 women (n-intervention = 22 and n-control = 24) were included in the analyses. | Mean depression scores before intervention in both groups were the same. | The study did not include support from family and husband as an important factor in postpartum depression. |
| Sun et al., 2019 [ | Not applicable | Study protocol—no results reported. | None reported |
| Zhang et al., 2017 [ | Not applicable | 14 applications are specifically focused on postnatal depression and were reviewed. | Authors identified applications from Apple or the Android application stores, potentially missing out on other sources. |