Can a simple text message transform cancer care?
NCT ID NCT07745816
First seen Aug 04, 2026 · Last updated Aug 05, 2026 · Updated 1 time
Summary
This trial tests whether regular text-message check-ins can help advanced cancer patients get palliative care support earlier. Patients receive a text every two weeks asking them to rate their symptoms online. If any symptoms are concerning, a coordinator calls to assess and manage them. The goal is to improve quality of life and reduce hospital visits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A behavioral intervention: regular SMS text reminders to complete an online symptom questionnaire, with follow-up phone calls from a palliative care coordinator if symptoms are flagged.
- What this could lead to
- If effective, this approach could help advanced cancer patients receive earlier palliative care, improving quality of life and reducing hospital admissions.
- What could go wrong
- This is a relatively small trial, and the intervention depends on patient engagement with text messages and phone calls. It may not work for everyone or in all healthcare settings.
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 300 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 2029
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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21 to 120 years
- 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: * Inclusion criteria for patients: 1. 21 years old or older 2. Diagnosed of advanced cancer diagnosis, defined as metastatic or recurrent/ progressive Stage III/IV solid tumour 3. Has an unplanned hospital admission and expected to be discharged home 4. Able to speak English or Mandarin Chinese or Malay 5. Able to provide informed consent Additional inclusion criteria for patient participants of semi-structured interviews are: 6. Enrolled in the SPARKLE-2 RCT, whether randomized to the SPARKLE intervention or usual care group and regardless of fidelity to trial procedures. * Inclusion criteria for caregivers: 1. 21 years old or older 2. Self-endorsing or identified by an enrolled patient as a spouse/partner, relative or friend who knows them well and who provides support due to their cancer 3. Able to speak English or Mandarin Chinese or Malay 4. Able to provide informed consent * Inclusion criteria for healthcare providers: 1. 21 years old or older 2. Healthcare professional who is involved in the clinical care of patients with advanced cancer for at least 50% of their work hours 3. Able to provide informed consent 4. Involved in the processes of the SPARKLE-2 Exclusion Criteria: * Exclusion criteria for patients: 1. Assessed by the treating physician as unable to complete study procedures 2. Unable to complete patient-reported outcome measures * Exclusion criteria for caregivers: 1\. Unable to complete interviews * Exclusion criteria for healthcare providers: 1. Healthcare professionals that are not providing care for cancer patients. 2. Unable to complete interviews
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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
2 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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National Cancer Centre, Singapore
Singapore, 168583, Singapore
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Singapore General Hospital
Singapore, 169608, Singapore
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