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A single-center, prospective, single-blind, randomized controlled clinical trial to evaluate the efficacy and safety of digital therapeutics for post-operative patients with remote rehabilitation

A clinical study to evaluate the effect of post-operative functional recorvary and quality of life of digital therapeutics in early lung cancer patients

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049674
Enrollment
Unknown
Registered
2021-08-08
Start date
2021-08-01
Completion date
Unknown
Last updated
2022-04-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

lung cancer

Interventions

experimental group:use digital theraputics project to guide the post-operative rehabilitation exercise
control group:routine post-operative rehabilitation exercise guidance

Sponsors

Beijing Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The age at diagnosis is greater than 18 years and less than 75 years; 2. Lung cancer patients who underwent thoracoscopic lobectomy for lobectomy; 3. Can fill in the electronic questionnaire; 4. Be able to communicate with the investigator normally and complete the pulmonary function test.

Exclusion criteria

Exclusion criteria: 1. Has received neoadjuvant therapy; 2. The patient cannot return to the hospital for examination as required due to personal reasons; 3. Patients who cannot exercise for other reasons, such as severe arthritis; 4. Other circumstances that the investigator considers not eligible for enrollment.

Design outcomes

Primary

MeasureTime frame
recovery of postoperative pulmonary function;quality of life;

Secondary

MeasureTime frame
recovery of postoperative pulmonary function;borg score;pain score;emergency admission rate;postoperative complications;

Countries

China

Contacts

Public ContactWu Nan

Beijing Cancer Hospital

nanwu@bjmu.edu.cn+86 13910154426

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026