Skip to content

Effects of Cassava wax hot bath in patients with plantar fasciitis: A randomized controlled trial

Effects of Cassava wax hot bath in patients with plantar fasciitis: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220128002
Enrollment
40
Registered
2022-01-28
Start date
2022-01-31
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with plantar fasciitis Plantar fasciitis, Cassava

Interventions

Cassava wax hot bath ,Paraffin wax bath
Experimental Other,Active Comparator Other
Cassava wax bath ,Paraffin wax bath

Sponsors

Thailand Science Research and Innovation (TSRI)
Lead Sponsor
School of Integrative Medicine, Mae Fah Luang University
Collaborator

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients with plantar fasciitis

Exclusion criteria

Exclusion criteria: A history of the following diseases or disorders: Neurological conditions, Inflammatory arthritis of lower limb, Contagious skin disease in the foot, Thrombophlebitis, fracture of lower limb, Inflammation of lower limb, Surgery on the lower limb, Sensory impairment of lower limb and Allergic to cassava starch

Design outcomes

Primary

MeasureTime frame
Current pain intensity Before and immediately after first treatment session,1 day after end of the intervention period, 1 month and 3 months after end of the intervention period Current pain intensity measured using visual analog scale

Secondary

MeasureTime frame
Pressure pain threshold Before and immediately after first treatment session,1 day after end of the intervention period, 1 month and 3 months after end of the intervention period Pressure pain threshold measured using algometry,Pain frequency Before the first treatment session,1 day after end of the intervention period, 1 month and 3 months after end of the intervention period Pain frequency measured pain frequency questionnaire ,Ankle dorsiflexion range of motion Before and immediately after first treatment session,1 day after end of the intervention period, 1 month and 3 months after end of the intervention period Ankle dorsiflexion range of motion measured using goniometer,The Foot and Ankle Ability Measure (FAAM) Before and immediately after first treatment session,1 day after end of the intervention period, 1 month and 3 months after end of the intervention period the Foot and Ankle Ability Measure (FAAM) measured using FAAM questionnaire,Patient satisfaction 1 day after end of the intervention period Patient satisfaction measured using Patient satisfaction questionnaire,Side effect 1 day after end of the intervention period Side effect measured using side effect questionnaire

Countries

Thailand

Contacts

Public ContactVitsarut Buttagat

Mae Fah Luang University

vitsarut.but@mfu.ac.th0882674423

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026