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Effects of zinc and vitamin D separately and in combination on mood in overweight and obese subjects

Effects of zinc and vitamin D separately and in combination on mood, cortisol, tryptophan—kynurenine pathway, BDNF and hs-CRP in overweight and obese subjects

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201601252394N31
Enrollment
140
Registered
2016-10-31
Start date
2016-10-01
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

obesity. Simple obesity NOS

Interventions

Intervention 1: vitamin D- 2000 IU /day for 12 week zinc- 30 mg/day for 12 week. Intervention 2: zinc Placebo- 30 mg/day for 12 week vitamin D Placebo- 2000 IU/day for 12 week. Intervention 3: vitamin
Treatment - Other
Placebo
Treatment - Drugs
vitamin D- 2000 IU /day for 12 week zinc- 30 mg/day for 12 week
zinc Placebo- 30 mg/day for 12 week vitamin D Placebo- 2000 IU/day for 12 week
vitamin D 2000 IU/day for 12 week and zinc placebo for 12 week
zinc 30 mg/day 12 week and vitamin D placebo for 12 week

Sponsors

Vice Chancellor for Research, Iran University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria:age between 20 to 60 years old; BMI > 27; willing to participate; weight stable in 3 last months. Exclusion criteria: Having a history of coronary artery disease; acute or chronic renal failure; acute or chronic hepatic failure; presence of any chronic inflammatory and autoimmune disease; and any known malignancy; hormone therapy; Other non-pathological exclusion criteria included pregnancy; breast feeding; post-menopause; smoking, professional athlete; uncontrolled thyroid disorder; use of medications for dyslipidemia or hypertension; having a special diet for any reason prescribed by the clinic dietitian; consumption of nutritional supplements within the past 8 weeks.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Mood. Timepoint: At baseline and after weeks 12. Method of measurement: Beck Depression Inventory.;Serum cortisol. Timepoint: At baseline and after weeks 12. Method of measurement: ELISA.;Serum tryptophan. Timepoint: At baseline and after weeks 12. Method of measurement: ELISA.;Serum kynurenine. Timepoint: At baseline and after weeks 12. Method of measurement: ELISA.;Serum BDNF. Timepoint: At baseline and after weeks 12. Method of measurement: ELISA.

Secondary

MeasureTime frame
Serum hs-CRP. Timepoint: At baseline and after weeks 12. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomaye Yosaee

Department of Nutrition, School of public Health, Iran University of Medical Sciences

s_yousai2006@yahoo.com+98 21 8670 4805

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026