Skip to content

The effects of interdisciplinary early rehabilitation in post-operative patients with glioma: a randomized controlled clinical trial

The effects of interdisciplinary early rehabilitation in post-operative patients with glioma: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021528
Enrollment
Unknown
Registered
2019-02-25
Start date
2019-03-01
Completion date
Unknown
Last updated
2019-03-04

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

Conditions

Glioma

Interventions

1:early rehabilitation treatment
2:usual care treatment

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) aged = 18 years; (2) met with the World Health Organization (WHO) of glioma diagnostic criteria (2016 version); (3) the Karnofsky functional status score (KPS) = 70; (4) before the inclusion, treated with surgery, CT showed that there is no risk of bleeding, pathologically confirmed diagnosis, the tumor was completely or largely resected after surgery; (5) physical movement, cognition, speech, swallowing and other dysfunction after surgery; (6) No obvious pain, vomiting and other symptoms of high intracranial pressure symptoms are observed after the operation; (7) compliance with the doctor's assessment, treatment and cooperate with the completion of the treatment, willing to sign the informed consent form

Exclusion criteria

Exclusion criteria: 1. have poor drug control of epilepsy and mental symptoms; 2. previous cerebrovascular disease or other lesions of the central nervous system, which led to dysfunction of limbs, cognition, speech and swallowing; 3. serious listening comprehension obstacles, can not follow the instruction with training; 4. brain metastatic tumor patients; 5. Patients with pulmonary infection; 6. the patient himself has no desire to recover.

Design outcomes

Primary

MeasureTime frame
Modified Barthel index scale (MBI);Lawton instrumental activity in daily life;

Secondary

MeasureTime frame
Modified Rivermead movement index;

Countries

China

Contacts

Public ContactCHENGSEN JIA

Rehabilitation Center, West China Hospital, Sichuan University

13398184656@163.com+86 13398184656

Outcome results

None listed

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