Safety study of Depression Auxiliary Intervention Treatment Software (WL-iCBT) in depression
This study is completed in China. It is testing Depression Auxiliary Intervention Treatment Software (WL-iCBT) for depression.
DepressionBehavioralFrom 18 Years to 60 Years
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
Then choose your country and confirm availability with each study site.
In plain English
Key information made simple
What is this study testing?
This study is testing whether cognitive behavioural therapy may be useful for adults experiencing depression.
What would participation involve?
Participants may take part in cognitive behavioural therapy, attend study visits with the research team. The protocol may also involve randomization, placebo, or a comparison group. The registry lists locations in China.
Who is it mainly for?
This study appears to be mainly for adults with depression.
What should you check before joining?
Ask about how many sessions are required and who delivers them, whether there is placebo, randomization, or a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.
Your next step
Check the study details
Check the official source, then confirm these points with the research team.
Where are visits, can any be remote, and how much time is needed?
Costs and support
What costs, reimbursement or compensation apply?
Before joining
Questions to ask before joining
What are the exact eligibility criteria, and what could exclude someone?
How many visits, assessments, or follow-ups are expected, and over what period?
What risks, side effects, practical burdens, or alternatives should be understood first?
Who should be contacted to confirm locations, timing, compensation, and next steps?
Study clarity
Things to check before joining
Study start dateStarted: April 21, 2023
Recruitment status
Completed
Enrollment listed in the registry
315
Sponsor
Adai Technology (Beijing) Co., Ltd.
Sponsor type
Other organization
Study type
Behavioral
Intervention type
DEVICE
Study phase
Not clearly listed
Locations
China
Age range
From 18 Years to 60 Years
Official registry ID
NCT05554289
Official title
Efficacy, Safety, and Acceptability of Internet-based Cognitive Behavioral Therapy Delivered Via Smartphone for Mild-to-moderate Major Depressive Disorder: a Multi-center, Double-blind, Randomized Controlled Trial
Ask HopeStage to help me review this study
This record does not confirm open recruitment. We can help you understand it and explore other studies.
Study ID: NCT05554289. We help you review the study, but cannot decide medical eligibility.
Check recruitment and locations
Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.
The overall study status can differ from each site's status. Open a country to see its locations and their registry status.
China · 11 sites
Shenzhen Kangning Hospital
Shenzhen, Guangdong
Site status: Not listed — confirm with the team
The Fifth Affiliated Hospital of Sun Yat-sen University
Zhuhai, Guangdong
Site status: Not listed — confirm with the team
The First Hospital of Hebei Medical University
Shijiazhuang, Hebei
Site status: Not listed — confirm with the team
Zhumadian Second People's Hospital
Zhumadian, Henan
Site status: Not listed — confirm with the team
The Second Xiangya Hospital of Central South University
Changsha, Hunan
Site status: Not listed — confirm with the team
The First Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shannxi
Site status: Not listed — confirm with the team
Chengdu Fourth People's Hospital (Chengdu Mental Health Center)
Chengdu, Sichuan
Site status: Not listed — confirm with the team
The First Affiliated Hospital of Kunming Medical University
Kunming, Yunan
Site status: Not listed — confirm with the team
Zhejiang Provincial Tongde Hospital
Hangzhou, Zhejiang
Site status: Not listed — confirm with the team
Ningbo Kangning Hospital
Ningbo, Zhejiang
Site status: Not listed — confirm with the team
Quzhou Third Hospital
Quzhou, Zhejiang
Site status: Not listed — confirm with the team
In practice
For you
Participation may contribute to research. Personal benefit is not guaranteed.
Ask the research team to explain the activities, time commitment, and follow-up involved.
Study sites are listed. Confirm the relevant site and any travel before making plans.
Important
Not medical advice
Information from public sources.
Are you the study sponsor? Contact us to update this page: hi@hopestage.com
FAQ
Questions about this study
What is this study trying to understand?
This study is exploring psychotherapy or therapy for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.
What is a behavioral study?
This appears to be a behavioral / psychological / psychosocial study involving Depression Auxiliary Intervention Treatment Software (WL-iCBT), Placebo Control Software (WL-iHE). Phase is mainly useful to check for medication studies and some device studies.
Who might this study be for?
This study may concern people with depression; age range: From 18 Years to 60 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may take part in sessions or exercises related to habits, thoughts, emotions, or behaviors. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
Could this study affect my mood, habits, motivation, or stress?
Behavioral studies can involve habits, emotions, motivation, stress, sleep, or ways of thinking. Ask whether the intervention could affect your mood or stress, and who to contact if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by Adai Technology (Beijing) Co., Ltd., which appears to be another type of organization. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
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