| Literature DB >> 31803083 |
Jamie M Marshall1, Debra A Dunstan1, Warren Bartik1.
Abstract
One of the biggest growth areas in e-mental health resources has been the development and use of mobile mental health apps for smartphones and tablet devices. Such apps are being downloaded at increasing rates, but there have been questions about their efficacy and the research methodologies used to examine this. A review of the major app marketplaces, the Apple App Store and Google Play store, was conducted to locate apps claiming to offer a therapeutic treatment for depression and/or anxiety, and have research evidence for their effectiveness, according to their app store descriptions. App store descriptions were also analyzed to determine whether the app had been developed with mental health expert input; whether they had been developed in association with a government body, academic institution, or medical facility; and, whether or not they were free to download. Overall, 3.41% of apps had research to justify their claims of effectiveness, with the majority of that research undertaken by those involved in the development of the app. Other results indicated that 30.38% of shortlisted apps claimed to have expert development input; 20.48% had an affiliation with a government body, academic institution, or medical facility; and, 74.06% were free to download. Future research must consider other methodologies that may facilitate more research being completed on a greater number of apps, and future development needs to incorporate greater levels of input by mental health experts. Ways in which app stores could play a key role in encouraging more scientific research into the effectiveness of the mental health apps they sell are discussed.Entities:
Keywords: anxiety; app store; apps; depression; digital; e-mental health; mHealth; mental health
Year: 2019 PMID: 31803083 PMCID: PMC6872533 DOI: 10.3389/fpsyt.2019.00831
Source DB: PubMed Journal: Front Psychiatry ISSN: 1664-0640 Impact factor: 4.157
Coding used for app store search.
| Variable | Code | Description |
|---|---|---|
| Organizational affiliation | UNI | University. Produced in association with a university or other academic institution. |
| MEDC | Medical Center. Produced in association with a medical institution or hospital. | |
| GOVT | Government. Produced in affiliation with a government institution. | |
| INST | Institution. An explicit association (i.e. foundation, center, non-government organization, etc.). | |
| OTHER | Other. There is a clear but unclassifiable affiliation (e.g. a company), but not a “.com”. | |
| INSUFF | Insufficient. The affiliation cannot be confirmed by available information. | |
| Content source | EXP | Expert. Developed by/with an accredited medical or allied health professional, or a recognized institution. |
| EXT | External source. From a specific external source (e.g. DSM, recognized inventory, association etc.), but not based on or inspired by a theory/practice (e.g. CBT). | |
| LAY | Layperson. Source identified but no credential mentioned. Non-medical expertise clearly indicated by detailed bio or qualifier (e.g. years of experience). | |
| PLE | Person lived experience. Indication that the app is developed by a person with lived experience. | |
| INSUFF | Insufficient. No direct information provided about origin of information. |
Research evidence for the effectiveness of apps that offer a therapeutic treatment for anxiety and/or depression.
| Article | App name | Design | Participants | Outcome | Time/Length | Statistical analysis |
|---|---|---|---|---|---|---|
| Lee and Jung ( | Destressify | RCT | 77 participants in intervention group, 86 in waitlist control group; mean age 20.6 years | Stress, anxiety, and depression | Intervention period 4 weeks; no long-term follow-up | ANCOVA/MANCOVA; detailed in article |
| Christoforou et al. ( | Agoraphobia Free | RCT | 73 participants in intervention group, 69 in other app “control” group (no waitlist group), mean age 39.7 years | Anxiety (agoraphobia) | Intervention period 12 weeks; no long-term follow-up | Linear mixed model; detailed in article |
| Kinderman et al. ( | Catch It | Feasibility/pilot study | 285 participants (no control group); mean age 48.0 years | Positive/negative mood | Intervention period 6 weeks maximum, but varied amongst participants; no long-term follow-up | ANOVA; detailed in article |
| Carey et al. ( | Mindsurf | Feasibility/pilot study | 23 participants (no control group); no mean age given | Anxiety, depression | Intervention period 2 weeks; no long-term follow-up | ANOVA; inadequate detail in article |
| Kuhn et al. ( | PTSD Coach | RCT | 62 participants in intervention group, 58 in waitlist control group; mean age 39.0 years | Anxiety (posttraumatic stress disorder), depression | Intervention period 3 months; 3 months long-term follow-up | Repeated measures ANOVAs; detailed in article |
| Bakker et al. ( | MoodMission | RCT | 56 participants in intervention group 1, 56 in intervention group 2, 50 in intervention group 3, 64 in waitlist control group; mean age 34.0 years | Anxiety, depression | Intervention period 30 days; no long-term follow-up | ANOVA; detailed in article |
| Roepke et al. ( | SuperBetter | RCT | 93 participants in intervention group 1, 97 in intervention group 2, 93 in waitlist control group; mean age 40.2 years | Anxiety, depression, life satisfaction | Intervention period 4 weeks; 6 weeks long-term follow-up | Hierarchical Linear Modeling; detailed in article |
| Stiles-Shields et al. ( | Thought Challenger | RCT | 10 participants in intervention group 1, 10 in intervention group 2, 10 in waitlist control group; no mean age given | Depression | Intervention period 6 weeks; 4 weeks long-term follow-up | Repeated measures ANOVA; detailed in article |
| Flett et al. ( | Smiling Mind | RCT | 58 participants in intervention group, 67 in placebo control group; mean age 20.1 years | Stress, anxiety, depression, flourishing | Intervention period 40 days; no long-term follow-up | Multiple regression; detailed in article |
| Flett et al. ( | Headspace | RCT | 67 participants in intervention group, 67 in placebo control group (same control group as above study); mean age 20.1 years | Stress, anxiety, depression, flourishing | Intervention period 40 days; no long-term follow-up | Multiple regression; detailed in article |
*Independent research. RCT, Randomized controlled trial; ANOVA, Analysis of variance; ANCOVA, Analysis of covariance; MANCOVA, Multivariate analysis of co-variance.