A new recipe for cancer care: social prescriptions and Bite-Sized learning
NCT ID NCT07788729
First seen Aug 26, 2026 · Last updated Aug 27, 2026 · Updated 1 time
Summary
This pilot trial tests a new approach to support cancer patients and their caregivers. The intervention combines social prescriptions—connecting people to community resources—with short online learning modules and regular symptom check-ins. The goal is to see if this package can improve quality of life and help patients feel more in control of their care, particularly for those in underserved rural areas.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A multicomponent intervention combining social prescriptions, web-based micro-learning modules, and stepwise care based on symptom monitoring.
- What this could lead to
- If successful, this approach could offer a low-cost, scalable way to improve quality of life and care for cancer patients, especially those in rural areas.
- What could go wrong
- This is a pilot study, so results are preliminary and may not generalize. The intervention's complexity could also make it hard to implement consistently.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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About 384 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Nov 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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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Accepted
You do not need to have the condition being studied to take part.
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 for patients: * aged at least 18 years * primary diagnosis of early-stage or advanced-stage lung cancer, colorectal cancer, hematological neoplasm or malignant melanoma within the past 12 months * expected survival of at least 18 months * sufficient German language proficiency to complete questionnaires and interviews * attendance at the medical oncology units of participating hospitals * provision of written informed consent * ECOG Performance Status 0-2 * ability to name an eligible SP. Inclusion criteria for Support Persons: * being nominated by the patient as someone who provides support, encouragement or assistance in coping with their cancer * aged at least 18 years * proficiency in German * provision of written informed consent. Exclusion Criteria: Inability to * provide informed consent * independently complete interviews and/or questionnaires due to impaired speech, vigilance, or comprehension.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
6 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Charité - University Medicine Berlin
NOT_YET_RECRUITINGBerlin, Germany
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Faculty of Law, Business & Economics, Inst. for Healthcare Management & Health Sciences
ACTIVE_NOT_RECRUITINGBayreuth, Germany
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University Hospital Augsburg
NOT_YET_RECRUITINGAugsburg, Bavaria, Germany
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University Hospital Erlangen
NOT_YET_RECRUITINGErlangen, Bavaria, Germany
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University Hospital Köln
NOT_YET_RECRUITINGCologne, Germany
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University Hospital Regensburg
RECRUITINGRegensburg, Bavaria, 93053, Germany
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University Hospital Würzburg
NOT_YET_RECRUITINGWürzburg, Bavaria, Germany
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University Regensburg
ACTIVE_NOT_RECRUITINGRegensburg, Bavaria, 93053, Germany
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Other studies related to the condition(s) this trial covers.
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- A dose-escalation, dose-extension and efficacy-extension, phase I/II clinical study to evaluate the safety, tolerability, pharmacokinetic profile and preliminary efficacy of AP-L1898 capsule for the treatment of the patients with locally advanced or metastatic non-small cell lung cancer
- Phase III comparison of thoracic radiotherapy regimens in patients with limited small cell lung cancer also receiving cisplatin and etoposide
- Effects of a brief Mindfulness-Based chatbot intervention (Mindbot) on mindfulness level and stress among cancer patients: a randomized controlled trial
- Increasing equity in lung cancer screening
- Évaluation de la détresse post-traumatique relative au cancer dans l'année suivant le diagnostic chez les patients et les aidants et identification de leurs attentes envers un accompagnement personnalisé