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NCT06101589

Effect of Vitamin D Supplementation on Allostatic Load and Chronic Stress Along Line of Control in Azad Jammu Kashmir

Effect of Vitamin D Supplementation on the Allostatic Load and Chronic Stress Along Line of Control in Azad Jammu and Kashmir. Double Blind Randomized Placebo-controlled Trial
University of the Punjab·ClinicalTrials.gov·dietary supplementNot yet recruiting
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Study focus
Disease/Condition
Mental Health Issue
Drug/Device/Intervention
25 hydroxy cholecalciferol (Vitamin D) /25(OH)D3.
Study type
Interventional
Intervention type
dietary supplement
Sponsor & location
Primary sponsor
University of the Punjab
Location
Haveli, Pakistan
Timeline & enrollment
Phase
N/A
Start date
Nov 05, 2023
End date
Sep 15, 2024
Enrollment
120 participants
Primary outcome

Blood pressure,lipid profile,body mass index BMI

Summary

FULL TITLE Effect of vitamin D supplementation on the Allostatic load and Chronic stress
 along line of control in Azad Jammu and Kashmir. Double blind randomized placebo-controlled
 trial
 
 SHORT TITLE Effect of vitamin D supplementation on allostatic load and chronic stress along
 line of control in azad Jammu and Kashmir PROTOCOL/VERSION DATE 5th August 2023 METHODOLOGY
 Double blind randomized placebo-controlled trial
 
 STUDY DURATION 1 year STUDY CENTRES 1. District head quarter hospital haveli district Azad
 Kashmir 2. Rural health center (RHC) Khursheed Abad, 3. Basic health unit (BHU) Kirni
 Mandhaar and 4. First aid post (FAP) Chirikot. Main Objectives -To determine whether
 high-dose oral vitamin D supplementation effects allostatic load and chronic stress of the
 residents of line of control haveli district Azad Jammu and Kashmir (primary outcome)
 
 - To assess the prevalence and determinants of allostatic load and chronic stress among
 the residents of line of control (secondary outcome factors analysis).
 
 - To look into the relationship between chronic stress and vital clinical markers as blood
 pressure, BMI, and lipid profile in participants from line of control.
 
 - To determine whether this intervention is safe and well-tolerated by study participants
 (secondary outcomes, safety) No. of Participants 120 Statistical Methodology and
 Analysis The collected data will be analysed using appropriate statistical techniques:
 Descriptive statistics will summarize participant characteristics, chronic stress,
 psychological well-being, physical health indicators, and baseline vitamin D levels.
 Inferential statistics, such as t-tests, ANOVA, and regression analysis, will be used to
 examine relationships between chronic stress, allostatic load, vitamin D
 supplementation, and health outcomes. Subgroup analyses will explore potential
 interactions based on demographic variables

ICD-10 classifications
Mental disorder, not otherwise specifiedMental and behavioural disordersUnspecified mental disorderProblems related to certain psychosocial circumstancesProblems related to other psychosocial circumstances
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06101589
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06101589 through Pure Global AI's free database. This phase not specified trial is sponsored by University of the Punjab and is currently Not yet recruiting. The study focuses on Mental Health Issue. Target enrollment is 120 participants.

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