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Effectiveness of an integrated self-management program in patients with chronic plantar fasciitis

Effectiveness of an integrated self-management program on clinical-based outcomes in patients with chronic plantar fasciitis: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240923001
Enrollment
62
Registered
2024-09-23
Start date
2024-11-02
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

Interventions

Treatment through an integrated self-care program, which includes traditional Thai massage, stretching exercises, and strength training exercises, utilizing &#039
self-massage and foot exercise equipment&#039
.,Providing guidance and informational pamphlets on basic self-care for patients with plantar fasciitis.
Experimental Other,No Intervention No treatment
An integrated self-management program,Control group

Sponsors

Thailand Science Research and Innovation (TSRI)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Individuals with plantar fasciitis, exhibiting the following symptoms 1. Sharp pain in the heel that worsens with weight-bearing, especially in the morning after waking up during the first steps. 2. Current pain intensity (Visual Analog Scale) rated at 3 or higher. 3. Difficulty with heel movement. 4. Able to understand and follow the research process.

Exclusion criteria

Exclusion criteria: 1. Neurological disorders, including cerebrovascular accidents , spinal cord injuries, or other neurological conditions that impair the individual s ability to perform activities of daily living. 2. Fractures in the lower extremities. 3. Inflammatory conditions characterized by pain, swelling, redness, or heat in the lower extremities.

Design outcomes

Primary

MeasureTime frame
Current pain intensity Before the intervention, at the end of the intervention period, and one month after the intervention concludes Current pain intensity measured using visual analog scale

Secondary

MeasureTime frame
Pressure pain threshold Before the intervention, at the end of the intervention period, and one month after the intervention concludes Pressure pain threshold measured using algometry,Ankle dorsiflexion range of motion Before the intervention, at the end of the intervention period, and one month after the intervention concludes Ankle dorsiflexion range of motion measured using goniometer,The Foot and Ankle Ability Measure (FAAM) Before the intervention, at the end of the intervention period, and one month after the intervention concludes the Foot and Ankle Ability Measure (FAAM) measured using FAAM questionnaire,Side effect After the intervention period ends 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