Clinical research facility
Cardiff, CF14 4XW, United Kingdom
NCT Number: NCT05071365
This proof of concept and feasibility study will adopt a mixed methods approach. The primary objectives will be to assess participants' acceptance and usability of a package of self-help videos for Plantar Fasciitis designed to be accessed shortly after suitable participants are referred to the podiatry service, and also the feasibility of conducting a future randomised controlled trial. The secondary objectives will be to assess the effects of the intervention on pain and quality of life.
Looking for future studies?
Notify Me18 year–80 year
All sexes
Interventional
Not applicable
Cardiff, CF14 4XW, United Kingdom
This proof of concept and feasibility project will investigate the use of a self-help package of virtual resources for the treatment of plantar fasciitis. The research will involve a small group of ten, shortly after participants are referred to Cardiff & Vale UHB podiatry service and join the waiting list.
The virtual resources will include short videos demonstrating ways of managing symptoms, such as gentle stretching exercises, and footwear recommendations. Participants will be given access to these resources to watch at their convenience. Patient reported outcome measures (foot pain, and quality of life) will be collated at baseline and periodically up to 6 weeks. Participants' acceptability of these resources will be assessed through interviews at the end of the six weeks.
The feasibility of conducting a future randomised controlled trial will be assessed by looking at recruitment rates, retention and any patient safety issues. It is hoped the long term benefit will be that participants joining the waiting list can engage with these resources at the earliest opportunity to help manage their symptoms.
This research is important because it presents an opportunity to work with participants at the start of joining a waiting list, and the benefits of early access to virtual resources could be applicable to a number of different health problems.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
-
Inclusion criteria
Exclusion criteria
Single arm study. Participants are given access to self help videos for the management of plantar fasciitis while they are on the waiting list
Time frame: 6 weeks
End of study semi-structured interviews, analysed using a thematic approach.
Time frame: 6 weeks
End of study semi-structured interviews, analysed using a thematic approach
Time frame: 6 weeks
End of study assessment of feasibility through recruitment and retention rates.
Time frame: 6 weeks
End of study assessment of feasibility through adverse events
Time frame: 6 weeks
Patient reported outcome measures recorded at baseline, 2 4 and 6 weeks
Time frame: 6 weeks
Patient reported outcome measures at baseline, 2 4 and 6 weeks
Cardiff and Vale University Health Board
Other Gov
Early Access to Virtual Resources for the Self-management of Plantar Fasciitis: A Proof of Concept and Feasibility Study
Acronym: EASE-P
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06917937
Behavior, Fasciitis
Kütahya, Turkey (Türkiye)
View Trial DetailsNCT07078513
Fasciitis, Fasciitis, Plantar
Chakdara, KPK, Pakistan
View Trial DetailsNCT06523114
Arm Injuries, Elbow Injuries
Seoul, South Korea
View Trial DetailsNCT05622279
Fasciitis, Fasciitis, Plantar
Nantes, France
View Trial Details