Skip to content

Effect study of multicomponent exercise intervention based on planned behavior theory in patients with chemotherapy-induced painful peripheral neuropathy

Effect study of multicomponent exercise intervention based on planned behavior theory in patients with chemotherapy-induced painful peripheral neuropathy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101066
Enrollment
Unknown
Registered
2025-04-18
Start date
2025-04-18
Completion date
Unknown
Last updated
2025-04-21

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

Conditions

Patients with Gastrointestinal Tumors in Peripheral Neuropathy Induced by Pain Chemotherapy

Interventions

Intervention group:Usual care+multicomponent motion
Control group:Usual care

Sponsors

Affiliated Hospital of Jiangnan Universitys
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with histological or pathological diagnosis of digestive tract tumors. 2. Age >= 18 years old; 3. The chemotherapy regimen is paclitaxel or platinum neurotoxic chemotherapy drugs and subsequent chemotherapy requires at least 3 cycles; 4. According to the Total Neuropathy Score clinical version (TNSc) score > 0 and DN4 score >= 4 points; 5. Evaluated by the Physical Status Scale (ECOG), those with a score of = 41 were included in the study. 7. Possessing complete cognitive comprehension. 8. Informed consent to and voluntary participation in this study. 9. Patients can and do use electronic devices.

Exclusion criteria

Exclusion criteria: 1. Concomitant with diabetes, peripheral vascular disease, hypothyroidism, renal insufficiency, vitamin B12 deficiency, and neurological diseases (including stroke, Parkinson's disease, multiple sclerosis, and dementia); 2. The condition is critical; 3. Combined with other cancers, cancer brain metastases, craniocerebral trauma, mental illness, neurodegenerative diseases; 4. Patients receiving concurrent radiotherapy; 5. Those with exercise contraindications, such as lower extremity venous thrombosis and limited limb function; 6. Received or prepared for other interventions within 6 months.

Design outcomes

Primary

MeasureTime frame
NRS;CIPN symptoms;

Secondary

MeasureTime frame
Balanced capacity;Objective limb function test;Living quality;Exercise self-efficacy;exercise intensity;physical activity;

Countries

China

Contacts

Public ContactTeng Liping

Jiangnan University Hospital; Jiangnan University

teliping@jiangnan.edu.cn+86 159 5158 1260

Outcome results

None listed

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