Trial Outcomes & Findings for Role of Transcranial Direct Current Stimulation in Appetite and Weight Control (NCT NCT05609604)

NCT ID: NCT05609604

Last Updated: 2024-01-30

Results Overview

change in body weight in Kg measured from baseline at 5 weeks

Recruitment status

TERMINATED

Study phase

NA

Target enrollment

4 participants

Primary outcome timeframe

5 weeks

Results posted on

2024-01-30

Participant Flow

Participant milestones

Participant milestones
Measure
Active tDCS
This group will receive 30 minutes of active stimulation from tDCS tDCS: Electric current will be delivered to the pre-frontal cortex for 30 minutes.
Sham tDCS
This group will receive 30 minutes of sham (placebo) stimulation from tDCS Shame- No current
Overall Study
STARTED
2
2
Overall Study
COMPLETED
0
0
Overall Study
NOT COMPLETED
2
2

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Race and Ethnicity were not collected from any participant.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Active tDCS
n=2 Participants
This group will receive 30 minutes of active stimulation from tDCS tDCS: Electric current will be delivered to the pre-frontal cortex for 30 minutes.
Sham tDCS
n=2 Participants
This group will receive 30 minutes of sham (placebo) stimulation from tDCS Shame- No current
Total
n=4 Participants
Total of all reporting groups
Age, Continuous
48 years
STANDARD_DEVIATION 3 • n=2 Participants
43 years
STANDARD_DEVIATION 5 • n=2 Participants
45 years
STANDARD_DEVIATION 4 • n=4 Participants
Sex: Female, Male
Female
2 Participants
n=2 Participants
1 Participants
n=2 Participants
3 Participants
n=4 Participants
Sex: Female, Male
Male
0 Participants
n=2 Participants
1 Participants
n=2 Participants
1 Participants
n=4 Participants
Race and Ethnicity Not Collected
0 Participants
Race and Ethnicity were not collected from any participant.
Body mass index (BMI)
41 Kg/m2
STANDARD_DEVIATION 5 • n=2 Participants
38 Kg/m2
STANDARD_DEVIATION 4 • n=2 Participants
39.7 Kg/m2
STANDARD_DEVIATION 4 • n=4 Participants

PRIMARY outcome

Timeframe: 5 weeks

Population: no patient completed the study due to study termination due to departure of trained staff.

change in body weight in Kg measured from baseline at 5 weeks

Outcome measures

Outcome data not reported

Adverse Events

Active tDCS

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Sham tDCS

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Paresh Dandona

UBuffalo

Phone: 17168818924

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place