Reducing Ageism in Organizations: A Study Protocol (ageism)

March 16, 2026 updated by: Sara Jiménez García-Tizón, University of Salamanca

Reducing Ageism in the Workplace: Protocol for a Psychoeducational Programme in a Randomised Controlled Trial

Background: This article presents the protocol for a randomised controlled trial designed to develop and evaluate a psychoeducational intervention aimed at reduce ageism in the workplace, will improve attitudes toward older workers as well as various indicators of well-being and psychosocial functioning in the professional context.

Methods: The study will be conducted at the Faculty of Psychology of the University of Salamanca (Spain). Currently employed with at least five years of tenure in the organization or the relevant sector, performing tasks that involve frequent collaboration with colleagues from different generations will be recruited. Participants will be randomly assigned to two groups: the intervention group, which will undergo a psychoeducational programme consisting of 12 sessions over 3 months; and the control group, which will receive a educational programme of one session. All participants will complete initial and final assessments, as well as a 3-month follow-up, collecting sociodemographic data and applying various psychological, social and health assessment instruments.

Discussion: This protocol describes a comprehensive psychoeducational intervention aimed at reducing negative stereotypical beliefs about older workers and enhance relevant psychosocial variables in the organizational environment, such as job satisfaction, psychological flexibility, perceived social support, perceived health, and self-efficacy in navigating intergenerational work situations. The evidence generated will guide future interventions, policies, and educational programmes to promote preparing workers and teams in several key areas, such as recognising and challenging age-related stereotypes, developing empathy towards colleagues from different generations, promoting inclusive practices in daily interaction and work collaboration and fostering a more equitable and respectful organisational climate towards all ages.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

90

Phase

  • Not Applicable

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Currently employed with at least five years of tenure in the organization or the relevant sector. At this stage of their career, attitudes toward colleagues from different generations are considered more likely to be deeply ingrained, making this profile particularly suitable for the intervention.
  • Performing tasks that involve frequent collaboration with colleagues from different generations.
  • Ability and willingness to attend the program sessions regularly.

Exclusion Criteria:

Workers who meet any of the following conditions will be excluded from the study:

  • Significant reading or linguistic comprehension difficulties that prevent them from participating adequately in psychoeducational sessions or completing assessment instruments.
  • Serious and destabilised medical or psychological disorders that may interfere with the normal development of the programme (e.g., severe untreated depressive episodes, limiting neurological disorders).
  • Failure to meet the inclusion criteria, specifically not having been with the company for at least five years or not participating in intergenerational teams.
  • Refusal to sign the informed consent form or lack of availability to attend programme sessions regularly.

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

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Education Programme

Objective: Participants will receive general information and recommendations to foster inclusive attitudes towards older workers and promote a positive intergenerational work environment. This minimally active intervention provides basic support without the structured sessions of the psychoeducational programme, facilitating the comparison of effects between groups.

Materials: Dossier with instructions and recommendations on inclusion and intergenerational awareness at work.

Procedures: Participants will receive the dossier with information on: identifying age stereotypes, good practices for the workplace inclusion of older workers, and basic strategies for promoting a respectful and equitable work environment.

Participants will receive general information and recommendations to foster inclusive attitudes towards older workers and promote a positive intergenerational work environment. This minimally active intervention provides basic support without the structured sessions of the psychoeducational programme, facilitating the comparison of effects between groups.
Experimental: Psychoeducational Programme

Objective: The programme seeks to reduce stereotypes and negative attitudes towards older workers, promoting an inclusive and generationally diverse work environment. Its objectives include improving: attitudes towards older workers, psychological flexibility, perceived social support, well-being at work, perceived health, and self-efficacy in managing intergenerational teams.

Materials: Projector, computer, screen, presentations, stationery, chairs, tables, and homework log. Procedures: The programme combines structured education with psychoeducational activities. Who conducts it: All sessions are led by psychologists with experience in generational diversity and ageing in the workplace, rotating between three professionals to ensure consistency, thematic accuracy and personalised attention.

The programme seeks to reduce stereotypes and negative attitudes towards older workers, promoting an inclusive and generationally diverse work environment. Its objectives include improving: attitudes towards older workers, psychological flexibility, perceived social support, well-being at work, perceived health, and self-efficacy in managing intergenerational teams.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Attitudes toward older workers
Time Frame: Baseline; up to 24 weeks; 3 months follow up
Measured by the Stereotypes toward Aging at Work Questionnaire (CETV-T), adapted from the CENVE (Blanca et al., 2005). It consists of 20 self-administered items, with a 7-point Likert-type scale (from 1=strongly disagree to 7=strongly agree). It assesses four dimensions related to negative attitudes towards retirement: (1) health, (2) economy, (3) status and (4) leisure/family. The final scores indicate more negative attitudes the higher the value obtained. The full scale has a Cronbach's alpha of 0.80, for the factors, the values obtained are: Leisure/leisure time-family an alpha of 0.836, economy 0.791, status 0.78 and health 0.69 (although this factor has the lowest value it is still considered acceptable within psychometric research standards).
Baseline; up to 24 weeks; 3 months follow up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Job satisfaction and well-being at work
Time Frame: Baseline; up to 24 weeks; 3 months follow up
Measured using the Job Satisfaction Scale (JSS) adapted into Spanish (Lukas Mujika et al., 2016). The ESL consists of 15 self-administered items, answered on a 5-point Likert scale (from 1 = strongly disagree to 5 = strongly agree). Higher scores indicate greater job satisfaction and a more positive perception of an inclusive and intergenerational working environment.The scale demonstrates good overall reliability (Cronbach's alpha = 0.802) and has been validated using exploratory and confirmatory factor analysis.
Baseline; up to 24 weeks; 3 months follow up
Psychological flexibility
Time Frame: Baseline; up to 24 weeks; 3 months follow up
Assessed using the Acceptance and Action Questionnaire-II (AAQ-II) (Bond et al., 2011). The AAQ-II is a 7-item questionnaire designed to assess experiential avoidance and psychological inflexibility. Participants were asked to rate their agreement with each statement on a 7-point Likert scale, ranging from 1 (not at all true) to 7 (completely true). The reliability of this instrument in our sample was high (Cronbach's α = 0.949).
Baseline; up to 24 weeks; 3 months follow up
Perceived social support
Time Frame: Baseline; up to 24 weeks; 3 months follow up
Assessed using the MOS Questionnaire of Perceived Social Support (Sherbourne & Stewart, 1991). It assesses perceived social support. It consists of 20 items. It consists of five factors: support network, emotional/informational social support, instrumental support, positive social interaction and affective support. It has a Likert-type response format of 1 (never) to 5 (always) points. The overall scores range from 20 to 100 points. The higher the score, the more social support the individual perceives. It has a Cronbach's alpha reliability coefficient of 0.97.
Baseline; up to 24 weeks; 3 months follow up
Perceived health
Time Frame: Baseline; up to 24 weeks; 3 months follow up
Assessed using the Goldberg General Health Questionnaire (GHQ-12) (Goldberg & Williams, 1988; Spanish version of Sánchez-López & Dresch, 2008). It allows us to measure perceived health. It has 12 items with 4 response options, from 0 (better than usual) to 3 (much more than usual). Higher scores correspond to a higher level of perceived health. It has good internal consistency, with Cronbach's alphas varying between 0.82 and 0.86 (Goldberg & Williams, 1988); and the Spanish validation has a Cronbach's alpha of 0.76 (Sánchez-López & Dresch, 2008).
Baseline; up to 24 weeks; 3 months follow up
Self-efficacy
Time Frame: Baseline; up to 24 weeks; 3 months follow up
Assessed by the Escala de Autoeficacia Generalizada (EAG) (Baessler & Schwarzer, 1996). It assesses the stable feeling of personal competence to deal effectively with a variety of stressful situations. It consists of 10 items with four Likert-type response options from 1 (incorrect) to 4 (true). Scores range from 10 to 40 points. Higher scores indicate higher levels of self-efficacy. The scale obtained a Cronbach's alpha of 0.81.
Baseline; up to 24 weeks; 3 months follow up

Collaborators and Investigators

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

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)

September 1, 2026

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

December 1, 2027

Study Registration Dates

First Submitted

March 16, 2026

First Submitted That Met QC Criteria

March 16, 2026

First Posted (Actual)

March 19, 2026

Study Record Updates

Last Update Posted (Actual)

March 19, 2026

Last Update Submitted That Met QC Criteria

March 16, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

They will be made available to researchers in the document repository "GREDOS" of the University of Salamanca, Spain.

IPD Sharing Time Frame

Data will be available at the end of the study.

IPD Sharing Access Criteria

Open access for researchers.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • ICF

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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