Health TrialsbyHealthPanel

Sea Buckthorn Aqueous Infusion Impact

ConditionBody Compostition
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorUniversity of Veterinary and Animal Sciences, Lahore - Pakistan

About this trial

* A total of 60 overweight women (BMI 25-29.9 kg/m²), aged 18-50years, will be enrolled and randomized equally into intervention and control groups. The intervention group will consume a 5 g freshly prepared seabuckthorn aqueous infusion daily for 12 weeks, while controls maintain usual habits without supplementation. * The seabuckthorn aqueous infusion will be prepared by using 250mL of potable boiled water and then cooled to a lukewarm temperature (around 40-45°C). At this point, 5 g of seabuckthorn powder will be added, stirred thoroughly until fully dispersed, and consumed immediately. The infusion will be freshly prepared once daily and administered in the morning after breakfast.

Measurements will be conducted using the InBody 270, a validated bioelectrical impedance analyzer employed in this study to obtain accurate assessments of body weight, body mass index (BMI), waist-hip ratio, and visceral fat levels. The device offers segmental analysis and visceral fat estimation through non-invasive, standardized procedures, ensuring consistency and reliability in longitudinal tracking.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Sea buckthorn aqueous infusion

    Dietary supplement

    Sea buckthorn aqueous infusion prepared by using 5g powder in 250 ml water.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: 1Placebo comparator 1 intervention
Group B: 2Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Body weight

unit of measurement in kilograms will be measured by weight machine

Time frame
12 weeks
2

Body mass index

body mass index will be measured using body mass index calculator

Time frame
at the end of intervention (12 week)

Secondary outcomes

1

visceral fat

visceral fat will be measured using bioelectric impedance analysis

Time frame
at the end of intervention period (12 week)
2

waist-hip ratio

waist hip ratio will be measured using measuring tape

Time frame
at the end of intervention period ( 12 week)

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Veterinary and Animal Sciences, Lahore - Pakistan

Lead sponsor

Source ClinicalTrials.gov
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