Can a smartphone app help oral cancer patients recover faster?
NCT ID NCT07504809
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a remote rehabilitation app can improve shoulder and neck recovery in oral cancer patients who had neck dissection surgery. 80 patients are randomly assigned to either standard home exercise materials or the app, which provides daily reminders and lets patients send videos to their rehab team. Researchers measure shoulder function and neck-related quality of life before surgery and at 10 days, 1 month, and 3 months after.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- remote rehabilitation app and exercise videos
- What this could lead to
- If successful, this could provide an effective, convenient way for oral cancer patients to recover shoulder and neck function at home after surgery.
- What could go wrong
- This is a small, early-stage study with only 80 participants, so results may not apply to everyone. The app-based approach may not work for patients who are not comfortable with technology.
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 80 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Dec 2026
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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * Primary oral cancer patients with surgical indications who provided informed consent and underwent surgical treatment including neck dissection with spinal accessory nerve preservation. * Able to understand and provide informed consent for rehabilitation training, cooperative with training and required follow-ups. * No history of conditions affecting shoulder mobility, including scapulohumeral periarthritis, cervical spondylosis, myofascial pain syndrome, or rheumatic diseases. Exclusion Criteria: * Previous surgery or trauma in the neck and shoulder region, or prior neck lymph node dissection. * Pre-existing shoulder and neck pain, abnormal bilateral shoulder and neck range of motion, or abnormal muscle strength. * Severe systemic underlying diseases that prevent cooperation with examinations. * Underwent radical neck dissection or received postoperative radiotherapy or chemotherapy that may affect shoulder and neck mobility.
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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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.Department of Oromaxillofacial-Head and Neck Surgery, Department of Oral and Maxillofacial Surgery, School and Hospital of Stomatology, China Medical University, Liaoning Provincial Key Laboratory of Oral Diseases, Shenyang, PR China.
Shenyang, Liaoning, 110001, China
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