Trials / Unknown
UnknownNCT05310175
Efficacy of Acupuncture at Acupoints Group Around the Base of Skull for Post-Stroke Depression
Efficacy of Acupuncture at Acupoints Group Around the Base of Skull for Post-Stroke Depression: a Randomized Controlled Trial
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 98 (estimated)
- Sponsor
- China Academy of Chinese Medical Sciences · Academic / Other
- Sex
- All
- Age
- 40 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this trial is to evaluate the efficacy and safety of electroacupuncture at acupoints group around the base of skull for post-stroke depression.
Detailed description
98 eligible participants with post-stroke depression will be recruited and randomly assigned to the experimental group and the control group in a ratio of 1:1. Participants in both groups will receive electroacupuncture or placebo acupuncture treatment at acupoints group around the base of skull 3 times a week for 4 weeks, and followed up for 24 weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Electroacupuncture | Filiform needles (0.30×50mm, Hanyi brand, Beijing Medical Appliance, China) and the SDZ-V electric acupuncture (Suzhou Medical Appliance) apparatus will be used. After acupuncture at the acupoints group, the needle handle will be connected with the electrode of the electric acupuncture apparatus. |
| DEVICE | Sham acupuncture | Shallow needle insertion of 2-3 mm at sham acupoints without manipulation. |
Timeline
- Start date
- 2022-05-06
- Primary completion
- 2023-05-06
- Completion
- 2024-10-01
- First posted
- 2022-04-04
- Last updated
- 2023-09-06
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT05310175. Inclusion in this directory is not an endorsement.