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Efficacy comparison of home stretching program between manual and non-manual book in symptomatic relief of plantar fasciitis,A randomized controlled -trial

Efficacy comparison of home stretching program between manual and non-manual book in symptomatic relief of plantarfasciitis,A randomized controlled-trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210223005
Enrollment
15
Registered
2021-02-23
Start date
2020-11-23
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

patient with acute plantar fasciitis (symptomatic less than 10 months) plantar fasciitis stretching program

Interventions

participant with manual book assisted home stretching program (intervention
with instruction book),participipant without manual book assisted home stretching program (control
current standard of care)
Experimental Device,Experimental Device
manual book assisted home stretching program,participant without manual book assisted home stretching program

Sponsors

Investigator budget
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. participants who have an acute plantar fasciitis less than 10 months 2. participants who have a morning pain or a pain after a few moment of rest 3. participants who have diagnosed plantar fasciitis by orthopedics surgeon 4. age 18 to 60 years-old

Exclusion criteria

Exclusion criteria: participant who have underlying disease as follows rheumatoid arthritis SNSA gouty arthritis SLE participant who have pain on other area than medial calcaneal tubercle participant who have sensation problem in the foot participant who have been surgically treated around the foot participant who have a symptoms of compressive neuropathy participant who have been traumatized around the affected foot participant who have a history of NSAIDs allergy participant who is currently pregnant or breast feeding participant who is can not follow up visit as a protocol participant who can not follow the protocol

Design outcomes

Primary

MeasureTime frame
pain improvement in participant who follow the protocol within 8 week of follow up visit visual analog scale by patient report interview

Secondary

MeasureTime frame
foot functional improvement in participant who follow the protocol within 8 week of follow up visit patient report by questionnaire interview

Countries

Thailand

Contacts

Public ContactWeerapat Reepolmaha

Hatyai hospital

lee.weerapat@gmail.com0869599989

Outcome results

None listed

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