Skip to content

The impact of Transcutaneous electrical acupoint stimulation on postoperative sleep disorders in lung cancer patients under general anesthesia: a randomized controlled study

The impact of Transcutaneous electrical acupoint stimulation on postoperative sleep disorders in lung cancer patients under general anesthesia: a randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075751
Enrollment
Unknown
Registered
2023-09-14
Start date
2023-03-30
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Lung cancer

Interventions

Transcutaneous electrical acupoint stimulation group (TEAS group) :The patients in the TEAS group received transcutaneous electrical stimulation at bilateral Shenmen (HT7), Neiguan (PC6) and Sanyinjia
Control group:Only stick the electrode piece without stimulation

Sponsors

The Second Affiliated Hospital of Air Force Medical University (Tangdu Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective surgery for lung cancer; 2. Age 18-64 years old; 3. BMI 18-30kg/?; 4. ASA grade I to II; 5. Primary tumor without radiotherapy or chemotherapy before operation; 6. Agree to participate in this study and be able to fill in or answer the questionnaire independently.

Exclusion criteria

Exclusion criteria: 1. Lung cancer patients with pre-existing sleep disorders. Patients with apnea or snoring above moderate level; 2. Communication barriers and inability to cooperate with researchers; Have mental disorders or other diseases, recent use of antipsychotic, antidepressant drugs, etc.; 3. Have serious heart (cardiac function grade ? or above), lung, liver, kidney and other basic diseases; Or have recurrence metastasis, there are serious complications. 4. Confirmed/suspected history of alcohol, analgesic drugs or other drug abuse and addiction; 5. Percutaneous electrical stimulation is contraindicated, including local skin damage, infection or electrophysiological devices implanted in the body; 6. Participants in other clinical trials within 3 months before inclusion; 7. The doctor in charge or the researcher considers that there are other circumstances that are not suitable for participation in this study (reasons should be recorded).

Design outcomes

Primary

MeasureTime frame
The Pittsburgh sleep quality index (PSQI);Athens Insomnia Scale (AIS);

Secondary

MeasureTime frame
Blood gas analysis;Hemodynamic index;Anesthesia time and operation time;Pain score;Extent of pulmonary resection;Postoperative Complications;The main factors affecting postoperative sleep quality;

Countries

China

Contacts

Public ContactGao Changjun

The Second Affiliated Hospital of Air Force Medical University (Tangdu Hospital)

gaocj74@163.com+86 133 7922 7869

Outcome results

None listed

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