A phone call a month: could a simple telehealth program lift caregiver depression?
NCT ID NCT07771413
First seen Aug 18, 2026 · Last updated Aug 21, 2026 · Updated 2 times
Summary
This pilot study tests whether a four-week telehealth program can reduce depressive symptoms in caregivers of children with cerebral palsy. Participants receive a behavioral intervention via telephone every four weeks, and their depression and anxiety levels are measured before and after. The goal is to see if this approach is feasible and might offer a practical way to support caregiver mental health.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A four-week telehealth behavioral intervention based on Lewinsohn's model of depression, delivered via telephone calls.
- What this could lead to
- If effective, this approach could offer a practical, low-cost way to support the mental health of caregivers of children with cerebral palsy.
- What could go wrong
- This is a very small pilot study (12 participants) with no control group, so results may not be generalizable. The intervention is brief and may not produce lasting effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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12 people
The number who actually took part.
- Started
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Nov 2025
- Finished
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Jan 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * have a child who diagnosed cerebral palsy * have adequate cognitive ability * 18 years or older * BDI score ≥3 Exclusion Criteria: * under 18 years old * BDI score \<3 * cognitive impairment * not being a caregiver of cerebral palsy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Gülhane Research and Education Hospital
Ankara, Ankara, 06000, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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