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UnknownNCT05346913

ICBT Program for Caregivers of Persons With SCI

This study has public registry information. It focuses on depression and currently lists study information.

Depression, Anxiety, ...BehavioralOver 18 Years
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Study ID: NCT05346913. We help you review the study, but cannot decide medical eligibility.
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, complete questionnaires or follow-up assessments, attend study visits with the research team.

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 a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.

What to expect

Your next step

The official record suggests a remote format run through a research setting. Participation appears to involve guided sessions or support activities with check-ins on how they fit into daily life. The main fit is usually matching the main diagnosis and having access to the required digital tools, while common reasons not to take part include safety concerns that need urgent care first and active substance or alcohol problems that could affect the results. The official record does not list a formal phase, which usually means this is focused more on feasibility, delivery, or support than a standard numbered clinical-trial phase.

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateEstimated: April 2024
Recruitment status
Unknown
Estimated enrollment
Not clearly listed
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Sponsor type
Research institute
Study type
Behavioral
Intervention type
Behavioral / psychological / psychosocial
Study phase
Not clearly listed
Locations
Not clearly listed
Age range
Over 18 Years
Official registry ID
NCT05346913
Official title
ICBT Program for Caregivers of Persons With SCI
Official source
Official registry link

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Study ID: NCT05346913. We help you review the study, but cannot decide medical eligibility.
In practice

For you

Taking part may help test a support approach in real life.

It requires regular follow-up, often through questionnaires or interviews.

Can be done remotely.

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 digital app or tool 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. Phase is mainly useful to check for medication studies and some device studies.

Do I need to want to stop or reduce tobacco use to participate?

The public registry appears to mention tobacco, nicotine, alcohol, cannabis, or another addiction-related topic. Ask the study team whether you need to want to stop, reduce, already be abstinent, or simply meet use-related criteria. Eligibility must be confirmed by the study team.

Does a loved one or caregiver need to be involved?

The public registry appears to mention a loved one, caregiver, or family involvement. Ask whether that person must participate, provide information, attend visits, or simply be available if needed. The study team must confirm what is required.

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.

What practical constraints should I expect?

The likely practical burden appears very high. Things to check include multiple visits or assessments. Ask the study team about duration, visits, possible compensation, data access, and what happens if you want to stop.

Who is behind this study?

This study is sponsored by London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's, which appears to be a research institute. 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 recruitment status is not clearly listed. Check the official registry or contact the study team.

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