Tamil Version of Foot Function Index

Not Applicable

• Conditions: Health Condition 1: M709- Unspecified soft tissue disorder related to use, overuse and pressure

• Registration Number: CTRI/2023/11/059426
• Lead Sponsor: TSVeeragoudhaman

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Language proficiency: Participants should be native Tamil speakers or individuals fluent in Tamil, as they will be required to

understand and respond to the translated FFI questionnaire.

2. Age range: Specify the age range that is relevant to your study. For example, participants could be adults aged 18 to 65 years or a specific subgroup within that range.

3. Foot-related condition:

Include individuals who have a foot-related condition or injury that affects their foot function. This could include conditions such as

plantar fasciitis, ankle sprains, or other foot-related problems.

4. Clinical diagnosis: Participants should have received a clinical diagnosis of the foot-related condition from a qualified healthcare

professional. This ensures that participants have a confirmed condition that can be assessed using the FFI.

5. Willingness to participate: Participants should be willing to take part in the study and comply with the study procedures, including completing the translated FFI questionnaire and any follow-up assessments or interviews.

6. Ability to provide informed consent: Participants should have the capacity to understand the study purpose, procedures, and potential risks involved. They should be able to

provide informed consent or have a legally authorized representative who can provide consent on their behalf.

Exclusion Criteria

1. Inability to understand or communicate in Tamil: Participants who do not have sufficient proficiency in Tamil to understand the

translated FFI questionnaire or providing meaningful responses should be excluded.

2. Cognitive impairment: Individuals with severe cognitive impairment or neurological conditions that impair their ability to comprehend and

respond to the questionnaire accurately may be excluded.

3. Medical contraindications: Exclude individuals who have medical conditions or physical limitations that prevent them from completing

the FFI questionnaire or participating in the study procedures safely.

For example, individuals with severe foot deformities or amputations that significantly affect foot function may be excluded.

4. Participation in a similar study: Exclude individuals who have participated in a similar cross-cultural adaptation or translation study

of the FFI questionnaire to avoid duplicating data or potential bias from prior exposure to the instrument.

5. Concurrent participation in another research study: Exclude individuals who are currently participating in another research study that may interfere with their ability to fully engage in the pilot study.

6. Inability to provide informed consent: Exclude individuals who lack the capacity to understand the purpose, risks, and procedures of the study and cannot provide informed consent, or who do not have a legally authorized representative available to provide consent on their behalf.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain <br/ ><br>Disability <br/ ><br>Foot Function IndexTimepoint: Baseline and Forty eight hours later test and re-test reliability

Secondary Outcome Measures

Name	Time	Method
Range of motion of Ankle and Subtalar jointTimepoint: Baseline and seventy two hours