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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06070441
Other study ID # CHATBOT_NECK_PAIN
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 10, 2023
Est. completion date August 10, 2024

Study information

Verified date January 2024
Source University of Valencia
Contact David Hernández-Guillén
Phone +34963983853
Email david.hernandez@uv.es
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project continuing to study on the effectiveness of a Chatbot in promoting adherence to home physiotherapy treatment for patients, in this case, with cervical musculoskeletal injuries and pain. The use of digital technologies and media is an important option to complement in-person treatment and promote adherence to treatment at home. The research aims to verify whether the use of a Chatbot as a means of communication can produce improvements in patient adherence and clinical results.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date August 10, 2024
Est. primary completion date July 10, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Over 18 years. - Diagnosis of cervical pain. - Indication of treatment through home exercises. - With a personal smartphone - Verbally confirms to have installed an instant messaging service or app, and accesses it at least 3 times a week Exclusion Criteria: - No to sign the informed consent. - Not able to understand, read and write in the Spanish language

Study Design


Related Conditions & MeSH terms

  • Neck Pain
  • Treatment Adherence and Compliance

Intervention

Other:
Education
One-week, three sessions in alternate days, outpatient supervised education on how to perform the exercises at home
Device:
Chatbot
12 week- intervention consisting of messages with an explanatory video of each exercise indicating how to do it and how many repetitions to perform
Other:
Home exercise, usual care
12 week- intervention. Printed sheets indicating how to exercises and how many repetitions to perform

Locations

Country Name City State
Spain David Hernández Guillén Valencia

Sponsors (1)

Lead Sponsor Collaborator
University of Valencia

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adherence Record of the number of sessions performed. 0 weeks, 12 weeks
Secondary Visual analogue scale (VAS) Numerical scale from 0 to 10, where 0 indicates no pain and 10 is the maximum pain experienced. 0 weeks, 12 weeks
Secondary Disability The Neck Disability Index (NDI) consists of ten questions in the following domains: Pain Intensity, Personal Care, Lifting, Reading, Headaches, Concentration, Work, Driving, Sleeping, and Recreation. Scoring: Each question contains six answer choices, scored from 0 (no disability) to 5 (complete disability). 0 weeks, 12 weeks
Secondary Satisfaction scale with the treatment received The CRES-4 satisfaction scale consists of four items designed to evaluate whether patients are satisfied with the therapy they have received and whether it has been perceived as effective. Its global score is intended to reflect treatment effectiveness as perceived by the patient. It is a good complementary tool to judge, in particular, satisfaction with the treatment received. Consists of four questions, and score with a score ranging from 0 to 18 points. The more points, the more satisfied you are with the treatment. 12 weeks
Secondary Sistem usability scale It consists of a 10 item questionnaire for measuring the usability of the experimental intervention tool with five response options for respondents, from Strongly agree to Strongly disagree 12 weeks
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