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Program evaluation of hemophilia society activities

Evaluation of support program extended to people with hemophilia: A multicentric mixed qualitative study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/10/046558
Enrollment
297
Registered
2022-10-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Health Condition 1: D67- Hereditary factor IX deficiency Health Condition 2: D66- Hereditary factor VIII deficiency

Interventions

None listed

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Persons with hemophilia, care givers (Mother, Fathers and close relatives) those associated for more than 2 years with the society, executive members of the chapters with >2 Years of experience as office bearer.

Exclusion criteria

Exclusion criteria: Females who are diagnosed with hemophilia, PwH who are not a member of a chapter, parents who are not living with PwH, non-residents of India.

Design outcomes

Primary

MeasureTime frame
The proposed study aims at exploring the day to day life and the impact of hemophiliacs being a part of the hemophilia societyTimepoint: 16 months

Secondary

MeasureTime frame
The evidence of the positive impacts made on the life of PwH and their family by the hemophilia societyTimepoint: 12 months

Countries

India

Contacts

Public ContactDr Sreejith Govindan

Melaka Manipal Medical College (Manipal Campus)

dinesh.nayak@manipal.edu9845226437

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026