Methodology for integrated data collection for the work
Not Applicable
- Conditions
- Health Condition 1: I10-I16- Hypertensive diseasesHealth Condition 2: F431- Post-traumatic stress disorder (PTSD)Health Condition 3: E119- Type 2 diabetes mellitus without complications
- Registration Number
- CTRI/2022/08/044835
- Lead Sponsor
- Gunjan Y Trivedi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
included
Exclusion Criteria
Participants with pre-existing illnesses such as recent acute coronary syndrome in the last three months, high grade of heart blocks, patients with pacemaker implantation or planned for implantation or any history of stroke or primary or secondary dysautonomia including diabetic neuropathy were excluded.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measure (a) Demographics (b) wellbeing (WHO-5), Anxiety (GAD-7), Depression (MDI), Sleep Quality (ISI), PTSD (Post Traumatic Stress Disorder) through PCL-C and ITQ (International Trauma Questionnaire)Timepoint: Baseline (before intervention), after 4 sessions, after 8 sessions, after 12 sessions -
- Secondary Outcome Measures
Name Time Method Qualitative insights from the PTSD pilotTimepoint: 3, 6, 12 months later where applicable