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Clinical Trials/CTRI/2018/08/015268
CTRI/2018/08/015268
Not yet recruiting
Phase 1

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.

Bayer Consumer Care AG0 sites0 target enrollmentTBD

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Bayer Consumer Care AG
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Eligibility 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

  • Not provided

Outcomes

Primary Outcomes

Not specified

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