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PsoriasisNCT01465061

A Survey on the Role and Benefits of Online Social Networks on Filipino Patients With Psoriasis

An observational study of Psoriasis, run by University of the Philippines.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

With the rise of usage of the internet, online social networks have recently been gaining popularity. Joining these groups can be beneficial to patients with chronic medical illness, such as psoriasis.This was a cross-sectional online survey of psoriasis patients in the Philippines who are members of online support… Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Psoriasis
What is being tested?
Online support group
How many people
124 participants
Where
No sites listed yet
Study dates
Feb 2011to Aug 2011
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 Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: Members of virtual psoriasis local support networks (Yahoo-based Psoriasis Philippine Online Community, Inc. and Facebook Psoriasis Online Support Group) will be the main subjects of the study.

Who may be able to join

  • diagnosis of psoriasis
  • individuals who are willing to complete the online survey
  • proficiency in English
  • membership in an online psoriasis support network

Who cannot join

  • nonmembers
  • unwilling to participate in the study

About this study

With the rise of usage of the internet, online social networks have recently been gaining popularity. Joining these groups can be beneficial to patients with chronic medical illness, such as psoriasis.This was a cross-sectional online survey of psoriasis patients in the Philippines who are members of online support groups. The survey was conducted for a period of three months.The purpose of the research project was to describe the demographics, disease characteristics, activities and benefits of online support groups to Filipino patients with psoriasis. The extent to which members experience empowering processes and outcomes was also evaluated.

Conditions
Psoriasis
Being tested
Online support group
Keywords
Online social network, Psoriasis, Filipino
Medical subject headings
Psoriasis

What participants receive

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

  • Online support groupBehavioural

    Also called Online social network, virtual online community

    Joining online support group

Study groups in NCT01465061
Study groupRoleWhat they receive
Online support userNot described
Receives: Behavioral: Online support group

What is being measured

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

  1. Demographic profile of online support users

    The sociodemographic profile of the respondents such as age (mean, range), sex, civil status, level of formal education, employment status were described.

    Measured: 3 months

  2. Disease characteristics of online support users

    The overall health status (poor, average, good), psoriasis severity (mild, moderate, severe), duration of illness of online support groups were evaluated.

    Measured: 3 months

Secondary outcomes (3)
  1. Activities performed and extent of participation of online support users

    Participants were also asked regarding their attitudes and experiences with online communities, length of use, log-on frequency and nature of online activities.

    Measured: 3 months

  2. Empowering processes and outcomes experienced by online support group members

    The frequency with which empowering processes (exchange information, find recognition, share experiences, encounter emotional support, help others) occurred were measured on a 3-point scale (1-seldom to never, 2-sometimes, 3-often). The outcomes experienced (are better informed, feel more confident in relationship with physician, have improved acceptance, feel more confident with treatment, have enhanced social well-being, have increased optimism and control over the future, have enhanced self-esteem) were assessed on a 3-point scale (1-disagree, 2-neither agree nor disagree, 3-agree).

    Measured: 3 months

  3. Correlation of variables

    Intervariable correlation (overall health status/psoriasis severity with frequency/duration of usage, educational level/employment status with frequency of usage) were also be assessed for significance.

    Measured: 3 months

Timeline

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

  1. First posted4 Nov 2011 (estimated)
  2. Study startFeb 2011
  3. Primary completionJun 2011
  4. Study completionAug 2011

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
Ecologic or community
Time perspective
Cross-sectional
Enrolment
124 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01465061
Sponsor's protocol ID
MED01032011
Status last verified
Nov 2011
First submitted
26 Oct 2011
Last updated
4 Nov 2011
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Psoriasis, run by University of the Philippines.

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 4 inclusion and 2 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: finished, as of the sponsor's last update on 4 Nov 2011. Status can change between updates, so confirm with the study contact before making plans.

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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Demographic profile of online support users (time frame: 3 months). 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 4 Nov 2011.

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