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Lung Neoplasms, Non Small Cell Lung Cancer / Patient Reported Outcome Measures / Postoperative Complications · Interventional Study
ClinicalTrials.gov · September 4, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a registered, actively recruiting randomized controlled trial designed to evaluate whether smartphone-based remote symptom monitoring with clinician feedback improves postoperative rehabilitation exercise adherence in lung cancer patients after video-assisted thoracic surgery. No results have been posted in this registry record; the trial includes a planned interim analysis due to slower-than-expected recruitment, and co-primary endpoints have been recently added by protocol amendment.
Interventional, Randomized, Parallel, Open label, Supportive Care purpose. Lung Neoplasms, Non-Small Cell Lung Cancer, Postoperative Complications, Patient Reported Outcome Measures, Telerehabilitation, Exercise Therapy; age from 18 Years; to 75 Years. Intervention: Intervention Group. Compared with: Control Group — No Intervention. n = 736. 1 site: China.
This is a registered, actively recruiting randomized controlled trial designed to evaluate whether smartphone-based remote symptom monitoring with clinician feedback improves postoperative rehabilitation exercise adherence in lung cancer patients after video-assisted thoracic surgery. No results have been posted in this registry record; the trial includes a planned interim analysis due to slower-than-expected recruitment, and co-primary endpoints have been recently added by protocol amendment.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
This is an active recruitment registry record with no results posted; it describes a planned RCT with an interim analysis framework but reports no efficacy data, outcomes, or effect estimates.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT05990946). This is a study registration, not published results. Lead sponsor: Zhongshan People's Hospital, Guangdong, China. Recruitment status: RECRUITING. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 736 participants (ESTIMATED). Conditions: Lung Neoplasms, Non-Small Cell Lung Cancer, Postoperative Complications, Patient Reported Outcome Measures, Telerehabilitation, Exercise Therapy. Interventions: DEVICE: ePRO based Remote Symptom Management provide by a mobile phone app. Primary outcome measures: Rehabilitation exercise adherence rate over 1 month after discharge , From the day of discharge to 30 days after discharge; Mean weekly exercise duration over 1 month after discharge , From discharge to 30 days after discharge.. Brief summary: Brief Summary: This randomized controlled trial aims to evaluate whether active remote symptom monitoring and management via a smartphone app utilizing electronic patient-reported outcomes (ePRO) can improve adherence to prescribed outpatient pulmonary rehabilitation exercises among postsurgical lung cancer patients. Eligible patients will use the app for perioperative care and be randomized to an intervention group receiving ePRO-based symptom monitoring with clinician feedback or a control group receiving ePRO without feedback. The primary outcome is rehabilitation exercise adherence rate over 1 month after discharge. If proven effective, the app-enabled remote rehabilitation model can be scaled up to enhance recovery for more postoperative patients. Due to slower-than-expected recruitment, an interim analysis was introduced through a protocol amendment. Before any unblinded between-group efficacy analysis, a blinded review of recruitment progress, data completeness, and outcome-data structure was conducted. Mean weekly exercise duration was subsequently added as a co-primary endpoint to complement the threshold-based exercise adherence outcome. The amendment and revised interim statistical framework were approved by the Ethics Committee before the formal interim analysis and incorporated into the updated study record.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.