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Impact of lunch provision on the nutritional and health status of female garment workers: A randomized controlled intervention trial for six months in Phnom Penh, Cambodia

Impact of lunch provision on the nutritional and health status of female garment workers: A randomized controlled intervention trial for six months in Phnom Penh, Cambodia - LUPROGAR

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00007666
Enrollment
360
Registered
2015-01-09
Start date
2015-04-07
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

E40-E46 E50-E64

Interventions

Group 1: Intervention group: A standard lunch will be served daily (6days/week for 6 month) through a canteen run by a Cambodian caterer. The meal will typically consist of local available food items

Sponsors

Justus-Liebig-University GiessenInstitute of Nutritional Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Nulliparous and non-pregnant female garment workers aged 18-30 years.

Exclusion criteria

Exclusion criteria: Chronic disease requiring treatment and/or medication. Subjects with handicaps or genetic disorders interfering with their nutritional and health status, severe anemia, signs of severe vitamin A deficiency and iodine deficiency.

Design outcomes

Primary

MeasureTime frame
Body weight: Measured at baseline and endline (after 6 month) to the nearest 0.01kg using a SECA-UNICEF scale (SECA, Hamburg, Germany).

Secondary

MeasureTime frame
BMI, triceps skinfold thickness & mid-upper arm circumference: Measured at baseline and endline. Body height will be measured using a calibrated height scale. A non-stretchable measuring tape will be used to measure mid-upper arm circumference. A skinfold caliper will be used to measure triceps skinfold thickness. Iron, VitA, folate & VitB12 status: Measured at baseline and endline. Ferritin, soluble transferrin receptor, C-reactive protein, alpha-1-acid glycoprotein and retinol-binding protein concentrations will be determined by enzyme-immunoassays. Plasma folate and vitamin B12 concentrations will be determined using a commercial radio-immunoassay. Elevated C-reactive protein & alpha-1-acid glycoprotein concentrations, will be used to indicate the presence of subclinical inflammation/infection. Anemia: Measured at baseline and endline. Using a HemoCue HB301 photometer (HemoCue, Ängelholm, Sweden). Handgrip strength: Measured at baseline and endline. Will be measured in a sitting position using a Jamar handgrip dynamometer (Lafayette Instruments). Morbidity: Measured at baseline, endline and after 3 months, using a pre-tested semi-quantitative questionnaire collecting data on illness history within the last 2 weeks prior the survey.

Countries

Cambodia

Contacts

Public ContactJan Makurat MSc

Justus-Liebig-University GiessenInstitute of Nutritional Sciences

jan.makurat@uni-giessen.de+49 641 99 39046

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 21, 2026