Needs Assessment Regarding "Mental Well-being-enhancing" Programs for Soon-to-be and (Recently) Retired Individuals

June 1, 2026 updated by: University Ghent

This study aims to improve understanding of the needs and well-being of individuals during the transition to retirement. The researchers seek to explore which activities and forms of support are perceived as helpful, which are already known or used, and which needs may currently remain unmet.

For the purpose of this study, "nearly or recently retired individuals" refers to people who are expected to retire within the next two years or who have retired within the past five years.

By examining participants' experiences and perceived needs during this transition period, the researchers aim to identify both existing strengths and potential gaps in the support currently available. Participants are invited to complete an online one-time questionnaire (10-15 minutes). The questionnaire includes questions about experiences related to the transition to retirement, awareness and use of activities or support initiatives, perceived strengths and limitations of these initiatives, and factors that may facilitate or hinder participation. The findings of this study may contribute to the development of recommendations to strengthen the support and resources available for (nearly) retired individuals in Flanders (Belgium).

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

500

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Ghent, Belgium
        • Flemish Centre of Expertise in Suicide Prevention, Ghent University
        • Contact:
        • Sub-Investigator:
          • Eva De Jaegere, PhD
        • Sub-Investigator:
          • Kirsten Pauwels, MSc
        • Sub-Investigator:
          • Pauline Stas, MSc
        • Sub-Investigator:
          • Ella Ballière, MSc
        • Sub-Investigator:
          • Marie Beyers, MSc

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Participants are adults who are "nearly or recently retired individuals". This refers to people who are expected to retire within the next two years or who have retired within the past five years.

Description

Inclusion Criteria:

  • Aged 18 years or older
  • Being within a period ranging from two years prior to retirement up to five years after retirement
  • Having access to the internet
  • Having sufficient proficiency in the Dutch language

Exclusion Criteria:

  • Not meeting the inclusion criteria

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Background information
Time Frame: Baseline. Completing the questionnaire will take about 10-15 minutes
Personal information (self-developed questionnaire): age, gender identity, cultural background, education level, financial situation (strained to comfortable), type of municipality (rural to large city).
Baseline. Completing the questionnaire will take about 10-15 minutes
Background information: transition to retirement and retirement status
Time Frame: Baseline. Completing the questionnaire will take about 10-15 minutes.
Questions on retirement status and transition (self-developed): current retirement status (yes/no and duration); work related stress before retirement (5 Likert scale questions); transition (unvoluntary/voluntary, early retirement, panned/unplanned); outlook on retirement (positive to negative)
Baseline. Completing the questionnaire will take about 10-15 minutes.
Experience with transition to retirement
Time Frame: Baseline. Completing the questionnaire will take about 10-15 minutes
self-developed questionnaire based on Floyd et al., 1992 and Wells et al., 2006: rating impact of 21 aspects on their transition to retirement (5-point Likert scale; no impact to very strong impact); emotional impact of retirement
Baseline. Completing the questionnaire will take about 10-15 minutes
Experience with retirement: language, framing and identity
Time Frame: Baseline. Completing the questionnaire will take about 10-15 minutes
self-developed questionnaire: preferred terminology (senior, elderly, retired,...); outlook on retirement (statements to be rated on 5-point Likert scale - totally disagree to totally agree)
Baseline. Completing the questionnaire will take about 10-15 minutes
Experienced needs
Time Frame: Baseline. Completing the questionnaire will take about 10-15 minutes
self-developped questionnaire: social netwerk (very broad social netwerk to feeling isolated); 9 domains to be rated on whether they needed support (needed and received, needed but did not receive, not needed);
Baseline. Completing the questionnaire will take about 10-15 minutes
Knowledge and use of existing support and resources
Time Frame: Baseline. Completing the questionnaire will take about 10-15 minutes
self-developed questionnaire: indicating to what degree (5-point Likert scale) they know, have used or would use a list of existing support resources (11 items). Open question for alternatives; framing: would they use these initiatives if directed at 'seniors' or 'elderly'; barriers to using existing resources (to be chosen from a list of 12 +14 +16 items or 'other'); facilitators to using existing resources (to be chosen from a list of 11 items or 'other'); preferences in activities or resources (format, to be chosen from a list of 7 items); to what degree do they find 3 new types of help appealing
Baseline. Completing the questionnaire will take about 10-15 minutes
Communication and implementation
Time Frame: Baseline. Completing the questionnaire will take about 10-15 minutes
self-developed questionnaire: through whom would they like to find out about activities or resources (7 options + 'other'); through which channels would they like to find out about activities or resources (7 options + 'other'); at what time of their transition to retirement would they like to find out about activities or resources (9 options)
Baseline. Completing the questionnaire will take about 10-15 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Gwendolyn Portzky, Flemish Centre of Expertise in Suicide Prevention (Ghent University)

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

May 26, 2026

Primary Completion (Estimated)

December 15, 2026

Study Completion (Estimated)

December 15, 2026

Study Registration Dates

First Submitted

June 1, 2026

First Submitted That Met QC Criteria

June 1, 2026

First Posted (Actual)

June 5, 2026

Study Record Updates

Last Update Posted (Actual)

June 5, 2026

Last Update Submitted That Met QC Criteria

June 1, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • ONZ-2026-0137

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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