Assessment of self reported physical symptoms, stress and anxiety social support, coping strategies among women carrier for hemophilia
Phase 1
- Registration Number
- CTRI/2018/08/015268
- Lead Sponsor
- Bayer Consumer Care AG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient reported outcomes such as physical symptoms, stress and anxiety, coping and social support.Timepoint: one time assessment
- Secondary Outcome Measures
Name Time Method ived experience among women carrier for hemophilia.Timepoint: 1 year