Condition category
Musculoskeletal Diseases
Date applied
24/05/2012
Date assigned
03/07/2012
Last edited
25/08/2016
Prospective/Retrospective
Retrospectively registered
Overall trial status
Completed
Recruitment status
No longer recruiting

Plain English Summary

Background and study aims
The Clinical Assessment Study of the Hand (CAS-HA) started in 2004 and participants have been followed-up every 18 months over 6 years. The study aims to describe the long-term course of hand pain, hand problems and hand osteoarthritis (pain/stiffness of the joints of the hand) in community-dwelling adults aged 50 years and over. Together with a linked study, this study also aims to look at associations between hand and knee osteoarthritis.

Who can participate?
Participants were originally recruited in 2004 and 2005 via questionnaire from the practice lists of two participating local General Practices. All those who indicated on the questionnaire that they experienced hand pain or hand problems in the previous 12 months and who provided consent to further contact were invited to attend for a clinical assessment. Participation at follow-up points has been restricted to those in the original cohort who consent to further contact.

What does the study involve?
The study involves completion of a questionnaire and attendance at a research clinic based within the local hospital for a clinical assessment and x-rays. The questionnaire consists of a Health Questionnaire, which asks about general health and hand problems, and a Regional Pains Survey, which asks about hip, knee and foot pain. The clinical assessment involves an interview, hand examination and assessment, digital imaging of the backs and fronts of both hands, and anthropometric measurement (height and weight). Participants are also assessed using a test of lower limb function. The clinical assessments will be carried out by a team of trained research therapists (occupational therapists and physiotherapists). Plain x-rays are taken of both hands and knees. Participants who do not wish to attend the research assessment clinics will be offered the opportunity to complete postal questionnaires only. Medical records will be reviewed in consenting participants. This is linked to a specific study objective to link osteoarthritis sub-types to GP consultation data in order to explore which hand pain and problems are presented to primary care over the follow-up period of 6 years.

What are the possible benefits and risks of participating?
As this is an observational study, there are no direct benefits for participants in relation to providing treatment or advice. The x-rays can be reported on by a consultant radiologist should the participant wish this, and the report sent to the GP. The risks from clinical assessment are negligible. Joint pain may be increased during examination, but the participant is fully informed of their rights to request that examinations are not done, and their right to withdraw from the study at any point. The main risk to the participant in this study is from exposure to radiation from the x-rays. The dose has been set by a radiation protection advisor and is relatively low (the equivalent to a few days natural background radiation). The risk from exposure to radiation from x-rays is covered in the Participant Information Sheet, which is sent to the participant prior to attending the research clinic, and is discussed fully during the consent process in the research clinic. Participants are informed that they can still participate in the study without having the x-rays taken.

Where is the study run from?
The Arthritis Research UK Primary Care Centre at Keele University, Staffordshire, England, UK

When is study starting and how long is it expected to run for?
October 2011 to August/September 2012

Who is funding the study?
The current stage of the study (6-year follow-up) is funded by Arthritis Research UK. Earlier stages of the study were funded by the Medical Research Council (MRC).

Who is the main contact?
Dr Helen Myers
h.l.myers@cphc.keele.ac.uk

Trial website

Contact information

Type

Scientific

Primary contact

Dr George Peat

ORCID ID

Contact details

Primary Care Musculoskeletal Research Centre
Keele University
Keele Road
Staffordshire
Newcastle-under-Lyme
ST5 5BG
United Kingdom
-
g.m.peat@cphc.keele.ac.uk

Additional identifiers

EudraCT number

ClinicalTrials.gov number

Protocol/serial number

11215

Study information

Scientific title

The course of hand pain, hand problems and hand osteoarthritis in community-dwelling adults aged 50 years and over: the 6-year follow-up of the Clinical Assessment Study of the Hand (CASHA)

Acronym

CASHA

Study hypothesis

The Clinical Assessment Study of the Hand (CAS-HA) is a longitudinal observational study of community-dwelling older adults aged 50 years and over with self-reported hand pain or hand problems. CAS-HA participants were recruited to the original cohort 6 years ago from the practice lists of two local general practices. Follow-up has been completed using postal questionnaires at 18-month intervals since then. At baseline, 623 people attended a local hospital for a clinical assessment and x-rays. Response rates to the postal follow-ups at 18-month intervals have been excellent. At the end of the last follow-up (54-months) there were 445 participants remaining in the cohort.

The 6-year follow-up study will involve consenting participants completing questionnaires and attending a research clinic at the local hospital for a clinical assessment and x-rays, very similar to the assessment at baseline. It is anticipated that the research clinics will commence in late August / early September 2011 and run for a maximum of ten months. All participants who will be approached for the 6-year follow-up have given consent to taking part in the study and to being contacted again. Of the 445 participants remaining in the cohort for the 6-year follow-up, it is anticipated that 430 will complete the questionnaires, and 325 will also attend for a clinical assessment.

Ethics approval

NRES Committee West Midlands – Solihull, 20/07/2011, ref: 11/WM/0196

Study design

Non-randomised observational cohort study

Primary study design

Observational

Secondary study design

Cohort study

Trial setting

Hospitals

Trial type

Screening

Patient information sheet

Not available in web format, please use the contact details below to request a patient information sheet

Condition

Musculoskeletal, All Diseases

Intervention

Seven plain x-rays will be taken of the hands and knees as follows: dorsi-palmar views of each hand and wrist, weight-bearing semiflexed posteroanterior (PA) view of both knees, and lateral and skyline views of each knee in a supine position with the knee flexed to 45 degrees.

Intervention type

Other

Phase

Not Applicable

Drug names

Primary outcome measures

Australian Canadian Hand Osteoarthritis Index (AUSCAN) measured at baseline

Secondary outcome measures

1. Anxiety and depression (HADS) measured at baseline
2. Current employment status measured at baseline
3. General health (SF-12) measured at baseline
4. Pain location (manikin) measured at baseline
5. Presence of hand pain and problems nodes, swelling, and participation restriction measured at baseline
6. Radiographic hand osteoarthrits (OA) measured at baseline
7. Radiographic knee OA measured at baseline
8. Symptom satisfaction measured at baseline

Overall trial start date

26/09/2011

Overall trial end date

27/07/2012

Reason abandoned

Eligibility

Participant inclusion criteria

1. Existing member of the CAS-HA cohort
2. Responded to the 3-year Follow-up Health Questionnaire
3. Provided written informed consent to further contact at 3-year follow-up stage
4. Male & female participants
5. Lower Age Limit 50 years

Participant type

Patient

Age group

Adult

Gender

Both

Target number of participants

475

Participant exclusion criteria

1. Participants who have died since 3-year follow-up
2. Participants who have become vulnerable (e.g. participants with known new-onset dementia, serious/terminal pathology) since their baseline assessment as judged by the lead GP at each practice
3. Participants who have withdrawn consent to further contact following the 3-year follow-up

We are keen to avoid upsetting or burdening participants and their relatives whose circumstances may have changed. Prior to any contacts being made for 6-year follow-up we will check to ensure that the mailing list contains no participants who have died. This means checking the mailing list at each practice. We are also including a screen of the mailing list by the lead GP at each practice to identify and exclude those participants who have become vulnerable since the screen was last conducted.

Recruitment start date

26/09/2011

Recruitment end date

27/07/2012

Locations

Countries of recruitment

United Kingdom

Trial participating centre

Keele University
Newcastle-under-Lyme
ST5 5BG
United Kingdom

Sponsor information

Organisation

Keele University (UK)

Sponsor details

Keele Road
Staffordshire
Newcastle-under-Lyme
ST5 5BG
United Kingdom

Sponsor type

University/education

Website

http://www.keele.ac.uk/

Funders

Funder type

Charity

Funder name

Arthritis Research (UK)

Alternative name(s)

Funding Body Type

Funding Body Subtype

Location

Results and Publications

Publication and dissemination plan

Not provided at time of registration

Intention to publish date

Participant level data

Not provided at time of registration

Results - basic reporting

Publication summary

Publication citations

Additional files

Editorial Notes

25/08/2016: No publications found, verifying study status with principal investigator.