Evidence map›Paper›PMID 39963546›Full record

ArticlePCN reports : psychiatry and clinical neurosciences2025

Movie- and mobile-therapy without therapist involvment for patients with obsessive-compulsive disorder: Protocol for a randomized controlled trial.

Hissei Imai, Yan Luo, Satoshi Funada, Takeshi Hashimoto, Kunitaka Matsuishi, Toko Takamatsu, Yasuo Yoshihara, Yayoi Hiraoka, Yasutaka Mizui, Yu Hayasaka and 5 more

Abstract read
In one paragraph

Article in PCN reports : psychiatry and clinical neurosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Hissei ImaiHealth Promotion and Human Behavior Kyoto University Graduate School of Medicine/School of Public Health Kyoto Japan.ORCID 0000-0003-3656-5188
Yan LuoCenter for Medical Education and Internationalization Kyoto University Graduate School of Medicine Kyoto Japan.
Satoshi FunadaHealth Technology Assessment Unit, Department of Preventive Medicine and Public Health Keio University School of Medicine Tokyo Japan.
Takeshi HashimotoHashimoto Takeshi Psychiatry Clinic Kobe Japan.
Kunitaka MatsuishiDepartment of Psychiatry Kobe City Medical Center General Hospital Kobe Japan.
Toko TakamatsuMomofuku Psychiatry Clinic Osaka Japan.
Yasuo YoshiharaYoshihara Psychiatry Clinic Nishinomiya Japan.
Yayoi HiraokaTakaraduka Psychiatry Clinic Takaraduka Japan.
Yasutaka MizuiFlower Road Psychiatry Clinic Takaraduka Japan.
Yu HayasakaHealth Promotion and Human Behavior Kyoto University Graduate School of Medicine/School of Public Health Kyoto Japan.
Nozomi TakeshimaHealth Promotion and Human Behavior Kyoto University Graduate School of Medicine/School of Public Health Kyoto Japan.
Haruko FukushimaDepartment of Psychiatry Kobe City Medical Center General Hospital Kobe Japan.ORCID 0000-0001-8616-8813
Kohei MatsudaDepartment of Psychiatry Kobe City Medical Center General Hospital Kobe Japan.
Takashi HashimotoDepartment of Psychiatry Kobe City Medical Center General Hospital Kobe Japan.
Toshi A FurukawaOffice of Institutional Advancement and Communications Kyoto University Kyoto Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Self-help programs without therapist involvement for obsessive-compulsive disorder (OCD) are promising, but the high dropout rate is a significant issue. Our software, which incorporates entertainment elements, showed a completion rate of over 80% in a pre-post comparison study, with superior effectiveness. This is the protocol for a study that aims to evaluate the efficacy and tolerability of a video-based mobile application for OCD treatment through a randomized controlled trial. Methods: This study is designed as a randomized controlled trial with two parallel group comparison, with assessors blinded to group allocation. The study will include outpatients aged 18 years or older diagnosed with OCD. The intervention group will receive a mobile-device-based intervention using an application grounded in cognitive behavioral therapy. The treatment period will be 8 weeks, during which 21 sessions will be conducted. Participants not allocated to the intervention group will be assigned to a waitlist control group for 8 weeks. The primary outcome for effectiveness will be the comparison of the Yale-Brown Obsessive Compulsive Scale. As the primary outcome for tolerability, participants in the intervention group who complete 80% or more of the sessions by the 8-week point will be defined as treatment completers, and the proportion of completers will be calculated. Assuming a 10% attrition rate, a total of 88 participants will be needed. Results: Results will be presented according to the protocol. Conclusions: If this study demonstrates that OCD can be improved through mobile-based self-help treatment without therapist involvement, it will become an important treatment option for patients.

Indexed as

adultanxiety disorderscognitive behavioral therapyinformation science categorypsychotherapy

Identifiers

PMID39963546
PMCPMC11830560

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.