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

Phase 1

Not yet recruiting

• Conditions: Women Carrier for Hemophilia

• Registration Number: CTRI/2018/08/015268
• Lead Sponsor: Bayer Consumer Care AG

Brief Summary

Data will be collected after obtaining informed consent from the participants. Women carriers of hemophilia will be identified through the registry of selected chapters of hemophilia society, Karnataka. Qualitative data collection will be carried out by a detailed interview through an audio recording till the data saturation happens.

Detailed Description

Not available

Study Timeline

• Study Start: 2018-08-13
• Last Update Posted: 2018-10-08

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: Female
• Target Recruitment: 384

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.	one time assessment

Secondary Outcome Measures

Name	Time	Method
Lived experience among women carrier for hemophilia.	1 year

Trial Locations

Locations (1)

Hemophilia Society, Kasturba Hospital, Manipal,; 🇮🇳 Udupi, KARNATAKA, India

Hemophilia Society, Kasturba Hospital, Manipal,

🇮🇳Udupi, KARNATAKA, India

sulochana

Principal investigator

9844995784

sulochana.k@manipal.edu