Trials / Recruiting
RecruitingNCT06598670
Transcranial Direct Current Stimulation on Post Stroke Depression
Effects of Transcranial Direct Current Stimulation on Post Stroke Depression
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 56 (estimated)
- Sponsor
- Riphah International University · Academic / Other
- Sex
- All
- Age
- 25 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The aim of the research is to address the critical gap that limited number of RCTs are conducted on this topic. To further explore the efficacy of tDCs, large sample sizes, large follow up period and rigorously controlled randomized clinical trials are necessary. An optimum stimulation protocol is also needed on this study. Previous studies lack information regarding effects of this stimulation on depression, cognition, quality of life in relation to different severity levels of stroke.
Detailed description
Research studies revealed that PSD causes both cognitive and physical impairments to lower motivation, which hinders rehabilitation program participation and slows down executive functions. Due to depression, cognitive dysfunctions difficulty in executive, working memory and emotional deficits which declines quality of life (QoL). Thus, the combined effects of cognitive decline and PSD considerably more worsen stroke survivors' QoL with regard to psychological, environmental and physical well-being Evidence supports various techniques for minimizing PSD, restoring cognitive function, and enhancing QoL including mindfulness-based therapies, exercise therapy (aerobic and resistance trainings), progressive muscle relaxation exercises, cognitive behavioral therapy (CBT). Non-invasive brain stimulation (NIBS) include transcranial direct current stimulations (tDCS) demonstrated significant therapeutic outcomes in the PSD rehabilitation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | tDCS | tDCS will be applied to the M1 area for 20 minutes with 5x7 cm electrodes. The intervention will be applied for eight weeks on alternate days |
| OTHER | Conventional treatment | Breathing exercises will be performed |
Timeline
- Start date
- 2024-10-25
- Primary completion
- 2025-06-30
- Completion
- 2025-07-31
- First posted
- 2024-09-19
- Last updated
- 2025-03-20
Locations
1 site across 1 country: Pakistan
Source: ClinicalTrials.gov record NCT06598670. Inclusion in this directory is not an endorsement.