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The Sukhshanti Study: Effect of a Sanitation Intervention on Women's Health

Not Applicable
Terminated
Conditions
Stress, Psychological
Interventions
Other: GSF Intervention
Registration Number
NCT02739178
Lead Sponsor
University of Oklahoma
Brief Summary

The study will measure the impact of sanitation access on women and girl's social and emotional health, behaviors, and quality of life in rural India before and after a sanitation intervention compared to a comparison group that will receive the same intervention at a later date.

Detailed Description

This mixed-methods, quasi-experimental study will evaluate the extent to which the Global Sanitation Fund (GSF) sanitation program in Bihar, India improves health and well-being among women and girls. Our study consists of a controlled before-and-after (CBA) study with an embedded ethnography.

Specific objectives are:

* Measure the effect of the GSF intervention on sanitation-related psychosocial stress (SRPS), generalized psychosocial stress (PSS), perceived quality of life, hair cortisol, and urogenital health among women between the ages of 14 and 65.

* Measure changes in sanitation adoption (e.g.: sanitation access and exclusive use) among individuals / households receiving the GSF intervention.

* Document individual and community experiences with sanitation, intervention participation, and latrine coverage through ethnographic methods.

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
1275
Inclusion Criteria
  • between 14 years to 65 years old
  • live in geographic area receiving GSF sanitation intervention in 2016
  • live in geographic areas matched to intervention communities
Exclusion Criteria
  • less than 25 years old and not reached menarche
  • greater than 25 years old and never married
  • refusal to participate

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
GSF Sanitation interventionGSF InterventionThis arm will receive the GSF sanitation intervention, a community-level sanitation intervention
Primary Outcome Measures
NameTimeMethod
Sanitation-Related Psychosocial Stress Scale (SRPS)12 month follow-up

The SRPS consist of 25 yes/no questions on experiences related to sanitation within the past thirty days of the date the SRPS is completed.This SRPS Scale specifically includes questions related to defecation, menstrual hygiene management, and post-defecation cleaning - the three behaviors that have the greatest contribution to sanitation-related psychosocial stress among women in India.

Secondary Outcome Measures
NameTimeMethod
Kessler Psychological Distress Scale (K10)12 month follow-up

The K10 provides a measure of non-specific psychological distress and consists of 10 items rated on a 5-point Likert scale (1 to 5). Scores are calculated by summing response across each item.

The WHO5 Well-Being Index (WHO-5)12 month follow-up

The WHO5 consist of 5 items rated on a 6-point Likert scale (0 to 5) related to subjective well-being, vitality, and mood.

Self-reported urogenital infections12 month follow-up

Urogenital infections, a health outcome linked to both menstrual hygiene management practices and sanitation access (Das et al., 2015) will be identified through self-report of any one of the following four symptoms: abnormal vaginal discharge (unusual texture / color and/or more abundant discharge than normal), burning or itching of the genitalia, burning or itching when urinating, or having genital sores.

Perceived Stress Scale (PSS10)12 month follow-up

A measure for non-specific perceived stress. The PSS10 is the short form of the PSS and consist of 10 items rated on a 5-point Likert scale (0 to 4). Scores are calculated by reverse scoring items with positive wording and summing across all items for a final score of 0 to 40. The PSS10 is not a diagnostic scale.

Hair cortisol12 month follow-up

Hair cortisol will be assessed in a sub-sample of women in both intervention and comparison communities.

Sleep duration12 month follow-up

Sleep duration will be assessed through a variety of self-report methods. The investigators will adapt questions from the Pittsburgh Sleep Quality Index that assess sleep duration over the past month: 1. During this past month, how many hours of actual sleep did the participant usually get at night? (Herring et al., 2013). The investigators will also ask the following questions: 1. To the best of the participant's knowledge, what time did the participant go to bed last night? 2. To the best of the participant's knowledge, what time did the participant wake up this morning?

Trial Locations

Locations (1)

NEERMAN

🇮🇳

Mumbai, India

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