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Can a smartphone app help gastric cancer patients recover faster after surgery?

NCT ID NCT07441850

Symptom relief Sponsor: Beijing Friendship Hospital Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jul 10, 2026 · Updated 3 times

Summary

This trial tests whether a smartphone-based program combining exercise, nutrition advice, and psychological support can reduce complications and improve recovery in 186 gastric cancer patients undergoing neoadjuvant therapy and surgery. Participants follow the program from before surgery until four weeks after discharge. The study compares this approach to standard care and also checks if the smartphone platform improves patient adherence compared to phone calls.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
perioperative multimodal rehabilitation program (exercise, nutrition, and psychological support) delivered via smartphone platform
What this could lead to
If successful, this could provide a practical, low-cost way to improve recovery and reduce complications after gastric cancer surgery.
What could go wrong
This is a relatively small, early-stage study testing a behavioral intervention, so results may not be generalizable. Adherence to the program could be low, and the smartphone platform may not work for all patients.

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

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

About 186 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2026

Expected to finish

Apr 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 70 years

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * patients aged between 18 and 70 years; * patients with histologically confirmed resectable adenocarcinoma of the oesophago gastric junction or stomach; * patients referred by a multidisciplinary team (MDT) for neoadjuvant therapy; * patients able to use a smartphone and the digital follow up platform, and willing to comply with regular follow up assessments; * patients who provide written informed consent. Exclusion Criteria: * presence of distant metastasis; * severe cardiopulmonary disease or other contraindications precluding completion of the 6MWT or participation in exercise training; * concurrent other malignant tumours; * suspected recurrent gastric cancer; * cognitive impairment, communication barriers, or psychiatric conditions that would prevent compliance with the study procedures; * women who are pregnant, lactating, or planning a pregnancy.

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Conditions

The condition(s) this trial relates to.

gastric cancer gastric neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Gastric cancer

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Beijing Friendship Hospital, Capital Medical University

    RECRUITING

    Beijing, China

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