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Chronic Ankle SprainNCT04960475

Study of Negative Emotion, Fear-Avoidance Belief and Quality of Life in Patients With Ankle Sprain

An observational study of Chronic Ankle Sprain, run by Peking University Third Hospital at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This study intends to investigate the negative emotions, fear-avoidance beliefs, and quality of life in patients with chronic ankle sprains to explore the relationship between negative emotions such as anxiety and depression, fear-avoidance beliefs, and their impact on quality of life. Read more about this study

Who is it for?
Ages 18 to 80 yearsHealthy volunteers can take part
Conditions the study is for
Chronic Ankle Sprain
What is being tested?
Hospital Anxious and Depression(HADS), Fear-Avoidance Belief Questionnaire (FABQ) and The MOS 36-Item Short From Health Survey (SF-36)
How many people
140 participants
Where
1 siteChina
Study dates
1 Jan 2021to 31 Dec 2021
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Ankle sprains are the most common injury in everyday life, military training and sports. Forty percent of people with ankle sprains develop chronic ankle instability, including mechanical ankle instability and functional ankle instability. Mechanical ankle instability is usually caused by structural changes in the ligamentous tissue around the ankle, kinematic damage, synovial changes or degenerative joint disease. Functional ankle instability refers to the subjective perception of instability during daily life or sports. Most patients do not require surgery, and clinical examination reveals only minor swelling and localized pressure pain, but rarely severe structural damage to the joint with limited range of motion and joint instability. However, many patients with chronic functional instability of the ankle joint due to ankle sprain are unable to resume normal work and life due to emotional anxiety and repeatedly seek medical attention.

Who may be able to join

  • Ankle sports injury time> 6 months;
  • age 18-50 years;
  • no pain in daily activities, or a numerical rating scale (NRS) 6 points or less;
  • no mechanical instability of the ankle joint and obvious restriction in joint movement ;
  • agree to participate in this study.

Who cannot join

  • acute inflammation of lower limb joints;
  • new or unhealed lower limb fractures;
  • history of lower limb surgery within 3 months;
  • lower limb pain caused by other diseases (such as lumbar disease, vascular disease, etc.);
  • speech and cognitive impairment
  • other diseases that cannot participate in this study.

Trial locations and contacts

1 site in 1 country.

China1 site
  • Peking University Third Hospital

    Beijing

Other trials in China

About this study

Official title: An Observational Study of the Relationship Between Negative Emotion, Fear-Avoidance Belief and Quality of Life in Patients With Chronic Ankle Sprain

This study intends to investigate the negative emotions, fear-avoidance beliefs, and quality of life in patients with chronic ankle sprains to explore the relationship between negative emotions such as anxiety and depression, fear-avoidance beliefs, and their impact on quality of life.

Read the detailed description

Research design: This study is an observational study. It is planned to recruit a total of 120 patients with ankle sprain injury who meet the selection criteria from the Rehabilitation Department of Peking University Third Hospital. They will be divided into an anxiety and depression group and a control group based on anxiety and depression scale. Basic information, anxiety and depression scales, fear-avoidance beliefs score and quality of life score of two groups will be compared and analyzed.

Being tested
Hospital Anxious and Depression(HADS), Fear-Avoidance Belief Questionnaire (FABQ), The MOS 36-Item Short From Health Survey (SF-36)

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Hospital Anxious and Depression(HADS)Other

    The assessment content in the scale is divided into two parts: anxiety and depression. Anxiety is an unexplained state of restlessness, manifested as tension, fear, and panic all day long. Depression is manifested as depression, slow thinking, decreased volition and physical symptoms. The two parts are scored separately. A total score of 0-7 means normal, a total score of 8-10 means mild depression/anxiety, a total score of 11-14 means moderate depression/anxiety, and a total score of 15-21 means severe depression/ anxiety.

  • Fear-Avoidance Belief Questionnaire (FABQ)Other

    FABQ is a self-assessment questionnaire with 16 options. Each option has 7 levels of 0-6 points, representing totally disagree, uncertain, and totally agree; there are 2 subscales, and one subscale measures the fear-avoidance in physical activity, another subscale measures fear-avoidance of work. The final score of FABQ is the superposition of the value of each item. A high score indicates a high level of fear-avoidance beliefs.

  • The MOS 36-Item Short From Health Survey (SF-36)Other

    The SF-36 is a multi-purpose survey designed to capture adult patients' perceptions of their own health and well-being. The SF-36 has 36 items grouped in 8 dimensions: physical functoning, physicial and emotional limitations, social functioning, bodily pain, general and mental health.

Study groups in NCT04960475
Study groupRoleWhat they receive
A/D groupChronic ankle sprain patient with anxity or depression
Receives: Other: Hospital Anxious and Depression(HADS); Other: Fear-Avoidance Belief Questionnaire (FABQ); Other: The MOS 36-Item Short From Health Survey (SF-36)
Control groupChronic ankle sprain patient with no emotional issues
Receives: Other: Hospital Anxious and Depression(HADS); Other: Fear-Avoidance Belief Questionnaire (FABQ); Other: The MOS 36-Item Short From Health Survey (SF-36)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. FABQ score

    the total score of Fear-Avoidance Belief Questionnaire

    Measured: 1 hr

  2. SF-36 score

    the score of SF36 questionnaire

    Measured: 1 hr

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Jul 2021
  2. Study start1 Jan 2021
  3. Primary completion31 Dec 2021 (estimated)
  4. Study completion31 Dec 2021 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
140 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04960475
Sponsor's protocol ID
M2021078
Status last verified
Jul 2021
First submitted
4 Jul 2021
Last updated
24 Nov 2021
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Chronic Ankle Sprain, run by Peking University Third Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 24 Nov 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

FABQ score (time frame: 1 hr). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Nov 2021.

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