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Assessment of self reported physical symptoms, stress and anxiety social support, coping strategies among women carrier for hemophilia

Assess the bio-psychosocial status (Physical symptoms, self-reported stress and anxiety and social support), coping strategies and lived experiences among women carrier for hemophilia: A mixed method approach.

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/08/015268
Enrollment
384
Registered
2018-08-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

None listed

Sponsors

Bayer Consumer Care AG
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Women carriers for hemophilia Study participants who are willing to give consent For qualitative approach, women who are having severe stress and anxiety and low coping, willing for audio recording

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Patient reported outcomes such as physical symptoms, stress and anxiety, coping and social support.Timepoint: one time assessment—

Secondary

MeasureTime frame
Lived experience among women carrier for hemophilia.Timepoint: 1 year—

Countries

India

Contacts

Public ContactSulochana Badagabettu

Manipal College of Nursing

sulochana.k@manipal.edu9844995784

Outcome results

None listed

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