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Clinical Trials/ISRCTN24104646
ISRCTN24104646
Completed
未知

Community Health And Medical Provision: Impact On Neonates (CHAMPION)

Effective Intervention (UK)0 sites0 target enrollmentMarch 20, 2007

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Effective Intervention (UK)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 20, 2007
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Effective Intervention (UK)

Eligibility Criteria

Inclusion Criteria

  • The trial site is the Nagarkurnool division of Mahabubnagar district in the Indian state of Andhra Pradesh. The trial will involve only those villages in the division with a population of less than 2,500 people. A woman is eligible for inclusion in the trial if she satisfies the following criteria: she is married, less than 50 years old, and resident in one of the 464 villages at the time of a baseline survey that is to be carried out immediately prior to randomization. Once the baseline survey has been carried out and the eligible women listed, the only permitted addition to the trial will be those women who marry into a trial village. Women will not be added or removed from the list as a result of either temporary or permanent migration from the village in which they are initially registered.
  • Only those children of eligible women whose estimated date of delivery at enumeration is at least six months after randomization will be included in the trial. As training and establishment of services in intervention villages will require time to be achieved, this lag in measurement is necessary to ensure exposure to the intervention.

Exclusion Criteria

  • Women and their children will be excluded from the trial if the woman in question is unmarried, if she is aged 50 or over at the time of the baseline survey or if she refuses to participate in the baseline survey.

Outcomes

Primary Outcomes

Not specified

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