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A Livelihood Intervention for Impoverished Women in Rural Uganda

Mass General Brigham logo

Mass General Brigham

Status

Unknown

Conditions

Indigency

Treatments

Other: Livelihood intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02619227
MH096620-S3

Details and patient eligibility

About

The objective of the study is to determine whether a livelihood intervention can improve economic and psychosocial wellbeing in rural Uganda.

Enrollment

92 estimated patients

Sex

Female

Ages

18 to 60 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women aged 18-60 years (or emancipated minors aged 16-17 years) who live with at least one child under the age of 5 in the same household
  • Women aged 18-60 years (or emancipated minors aged 16-17 years) who agree to participate in the livelihood intervention training program
  • Women aged 18-60 years (or emancipated minors aged 16-17 years) who agree to participate in study data collection

Exclusion criteria

  • Men
  • Women who do not live in Nyakabare Parish
  • Women under 18 years of age (if not emancipated minors) or older than 60 years of age
  • Women who do not live with at least one child under the age of 5 in the same household
  • Women who decline to participate in the livelihood intervention training program
  • Women who decline to participate in study data collection
  • Women who live in the same household as another study participant

Trial design

92 participants in 2 patient groups

Immediate treatment
Experimental group
Description:
Participants will receive a livelihood intervention package consisting of a orientation and training and a loan package of chickens and associated implements to create poultry microenterprises
Treatment:
Other: Livelihood intervention
Delayed treatment
No Intervention group
Description:
Participants will receive no intervention but will be placed on a waitlist to receive the intervention after a 12-month delay.

Trial contacts and locations

1

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Central trial contact

Alexander C Tsai, MD, PhD; Bernard Kakuhikire, MBA

Data sourced from clinicaltrials.gov

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