Can a Self-Help model ease cancer Patients' distress?
NCT ID NCT06674499
First seen Jun 24, 2026 · Last updated Aug 07, 2026 · Updated 2 times
Summary
This study tests a self-help rehabilitation model for people with head and neck cancer who are feeling anxious or depressed. Participants are randomly assigned to either the self-help program or standard care. The program includes three therapy sessions over eight weeks, led by a trained nurse. Researchers measure changes in emotional distress and quality of life using questionnaires and blood tests.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- self-help rehabilitation model based on cognitive-behavioral therapy
- What this could lead to
- If it works, this could provide a simple, therapist-guided program to help cancer patients manage anxiety and depression during recovery.
- What could go wrong
- This is a small, early-stage trial with only 144 participants, so results may not apply to all patients. The intervention is behavioral, so benefits may vary.
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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144 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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May 2026
- 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 to 70 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Pathologically diagnosed with head and neck malignancy. * Experiencing psychological distress. * Aged between 18 and 70 years. * Patients scheduled to receive antitumor treatment in a day hospital or outpatient setting. * ECOG performance status score of 0-2. * Patients voluntarily participate, fully understand, and are able to independently complete the questionnaires. Exclusion Criteria: * A history of other malignancies within the past 5 years. * A history of any mental illness, including but not limited to: generalized anxiety disorder, depressive disorder, panic disorder, schizophrenia, or bipolar disorder. * Patients currently receiving other psychological treatments or taking psychiatric medications.
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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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WestChina Hospital
Chengdu, Sichuan, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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