MedTrace Logo

A Progressive Resistance Training Program in Patients With Haemophilia

NCT02781233 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2018-10-18

No results posted yet for this study

Summary

This study evaluates the clinical impact of a progressive resistance training program in adults patients with haemophilia

Conditions

  • Haemophilia

Interventions

OTHER

Progressive resistance training

Progressive resistance training program

OTHER

Normal daily activities

Usual daily activities

Sponsors & Collaborators

  • Shire

    collaborator INDUSTRY

  • University of Valencia

    lead OTHER

Principal Investigators

  • Felipe Querol-Fuentes, MD, PhD · University of Valencia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-24
Primary Completion
2018-06-25
Completion
2018-06-25

Countries

  • Spain

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02781233 on ClinicalTrials.gov