Comparing Bowen Therapy and Tennis Ball Technique for Pain and Disability in Plantar Fasciitis Patients, A Randomized Controlled Trial
PF
Comparative Effects of Bowen Therapy and Tennis Ball Technique on Pain and Functional Disability in Patients With Plantar Fasciitis, A Randomized Controlled Trial
1 other identifier
interventional
80
1 country
1
Brief Summary
Plantar fasciitis is one of the most common causes of heel pain and can make everyday activities such as walking, standing for long periods, or climbing stairs difficult and uncomfortable. It usually occurs due to stress and inflammation in the plantar fascia, a thick band of tissue that supports the arch of the foot. People suffering from this condition often experience sharp pain, especially during the first steps in the morning or after long periods of rest. This study focuses on comparing two non-invasive treatment methods: Bowen Therapy and the Tennis Ball Technique. Bowen Therapy is a gentle manual therapy that uses soft rolling movements over muscles and connective tissues to reduce tension, improve circulation, and promote the body's natural healing process. On the other hand, the Tennis Ball Technique is a simple self-treatment method in which patients roll a tennis ball under the foot to massage the plantar fascia, relieve tightness, and reduce pain. The main purpose of this research is to determine which technique is more effective in decreasing pain and improving functional ability in patients with plantar fasciitis. By comparing these two methods, the study aims to provide a safe, affordable, and easy treatment option that can improve mobility, reduce discomfort, and enhance the quality of life of individuals suffering from heel pain.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 29, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 6, 2026
CompletedFirst Submitted
Initial submission to the registry
May 23, 2026
CompletedFirst Posted
Study publicly available on registry
June 1, 2026
CompletedJune 1, 2026
May 1, 2026
6 months
May 23, 2026
May 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
pain Intensity
Pain (VAS): Pain is the subjective experience of discomfort related to plantar fasciitis, measured using the Visual Analog Scale (VAS). Participants rate their pain on a 10-point scale from 0 (no pain) to 10 (worst possible pain), assessing pain at rest, during activity, and in the morning
Baseline and 12 weeks post intervention
Secondary Outcomes (1)
change in function disability
Baseline and 12 weeks post intervention
Study Arms (2)
Bowen Therapy Group
EXPERIMENTALParticipants in Group A will receive Bowen Therapy. The procedure will be as follows: 1. Frequency and Duration: Bowen therapy sessions will be conducted twice a week for a duration of 12 weeks. Each session will last approximately 30 to 45 minutes. 2. Treatment Focus: During each Bowen therapy session, the therapist will apply gentle and precise neuromuscular manipulations to specific anatomical points, focusing on the lower limb and foot. These points include fascial trigger spots and other myofascial tension areas that are implicated in plantar fasciitis. The Bowen technique involves rolling motions applied with the therapist's fingers or thumbs, working through the fascia and muscle tissues to promote fascial release, improve circulation, and reduce pain.
Tennis Ball Technique Group
EXPERIMENTALParticipants in Group B will perform self-myofascial release (SMR) using a tennis ball. The procedure for self-administration will be as follows: 1. Frequency and Duration: Participants will be instructed to perform the self-myofascial release (SMR) using a tennis ball once a day for 12 weeks. Each session will last about 10 to 15 minutes, with the participant rolling the tennis ball under the foot for about 5 to 10 minutes per foot. 2. Technique and Procedure: The participants will be taught the correct technique for rolling the tennis ball under the sole of the foot, with emphasis on applying appropriate pressure to trigger points or areas of tightness (e.g., arch, heel, and plantar fascia). A standardized pressure will be recommended to ensure the ball is rolled with sufficient force to produce fascial release without causing excessive discomfort or injury.
Interventions
Participants in Group A will undergo Bowen Therapy and the treatment will be provided twice weekly for 12 weeks, with each session lasting about 30 to 45 minutes, depending on individual response and condition. During each session, the therapist will apply gentle, targeted rolling movements using fingers or thumbs on specific points of the lower limb and foot. These points are selected based on areas of muscle tightness, fascial restriction, and pain related to plantar fasciitis. The technique aims to promote muscle relaxation, improve tissue circulation, and reduce pain by working on the fascial system and supporting overall neuromuscular balance
Participants in Group B will perform self-myofascial release (SMR) using a tennis ball. The procedure for self-administration will be as follows: 1. Frequency and Duration: Participants will be instructed to perform the self-myofascial release (SMR) using a tennis ball once a day for 12 weeks. Each session will last about 10 to 15 minutes, with the participant rolling the tennis ball under the foot for about 5 to 10 minutes per foot. 2. Technique and Procedure: The participants will be taught the correct technique for rolling the tennis ball under the sole of the foot, with emphasis on applying appropriate pressure to trigger points or areas of tightness (e.g., arch, heel, and plantar fascia). A standardized pressure will be recommended to ensure the ball is rolled with sufficient force to produce fascial release without causing excessive discomfort or injury.
Eligibility Criteria
You may not qualify if:
- History of injury in the lower limb within the last 6 months or surgery on the lower limb within the last 6 months. Known diseases which are systemic (or neurological) in nature (e.g., diabetes, rheumatoid arthritis, peripheral neuropathy). The use of corticosteroid injections or medications that disrupt the connective tissue has continued to be administered
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Alara Healthcare Wapda town Lahore
Lahore, Punjab Province, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Department of physical therapy
Alara healthcare Wapda town lahore
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principal Investigator
Study Record Dates
First Submitted
May 23, 2026
First Posted
June 1, 2026
Study Start
November 2, 2025
Primary Completion
April 29, 2026
Study Completion
May 6, 2026
Last Updated
June 1, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR
- Time Frame
- It will be available after the completion of the study
- Access Criteria
- Through the corresponding author
only IPD used in the results publication will be shared