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Creating and Testing a Weight Loss Program for Obese Women in Healthcare Centers

Development of obesity reduction program based on experiences and impact of obesity and evaluating its effectiveness on selected outcomes among obese women in selected healthcare settings - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110443
Enrollment
120
Registered
2026-05-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

None listed

Interventions

Intervention1: obesity reduction program: Information, Education, Communication (IEC). Digi alarm. Dietary Counseling. Aerobic exercises. Motivational Interviewing Control Intervention1: Nil: Nil

Sponsors

Sofiya Princess Hema.S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Obese women who belong to age group of 20 to 40 years. who are married and/unmarried. BMI of more than or equal to 25kg/m2. consent to adhere to the intervention regimen (Obesity Reduction Program) willing to participate in study. 6. who can speak English and/ Tamil

Exclusion criteria

Exclusion criteria: Obese women Who are contraindicated to the Obesity Reduction Program due to diseases such as arthritis& cardiovascular diseases. who are taking prescribed drugs for weight reduction Who are taking prescribed drugs for corticosteroids. Who were undergoing any kind of weight reduction program. With history of hormone therapy (steroids) and or use of oral contraceptives.

Design outcomes

Primary

MeasureTime frame
The study will highlight the perceived needs of obese women and barriers in weight management. The intervention will be beneficial to obese women in weight management.Timepoint: To evaluate the effectiveness of obesity reduction program at baseline 8 weeks 16 weeks and 24 weeks

Secondary

MeasureTime frame
To correlate knowledge quality of life selected anthropometric physiological & laboratory parameters of obese women. To associate the pretest level of knowledge quality of life selected anthropometric physiological & laboratory parameters of obese women with selected demographic variables. Timepoint: At baseline 8 weeks 16 weeks & 24 weeks

Countries

India

Contacts

Public ContactSofiya Princess HemaS

PSG College of Nursing

hemasofiya@gmail.com9884168324

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026