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Preparation for Sports Retirement: Study Protocol

Preparation for Sports Retirement: Protocol for a Psychoeducational Program in a Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07303504
Enrollment
26
Registered
2025-12-26
Start date
2026-02-01
Completion date
2027-05-01
Last updated
2025-12-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adaptation, Psychoeducation, Psychology, Psychosocial Factors, Retirement, Sport Retirement

Brief summary

Background: This article presents the protocol for a randomised controlled trial designed to develop and evaluate a psychoeducational intervention aimed at preparing high-performance athletes for the challenges and opportunities presented by the transition to retirement from sport. The protocol was developed through a literature review and consultations with experts in sports psychology and career transition. Methods: The study will be conducted at the Faculty of Psychology of the University of Salamanca (Spain). High-performance athletes aged 30 or older who are close to retirement or who have retired in the last five years 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 minimum 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 improving quality of life and attitudes towards retirement from sport, increasing life satisfaction, psychological flexibility, perceived social support, general health, self-efficacy and self-regulation, and reducing negative stereotypes associated with the end of a sporting career. The evidence generated will guide future interventions, policies, and educational programmes to promote a healthy, active, and satisfying transition to the post-sport stage.

Interventions

The program aims to facilitate a positive and healthy transition from elite sport to retirement. Its objectives include improving Quality of Life, Life Satisfaction, Psychological Flexibility, Perceived Social Support, Health, Self-Efficacy, and Self-Regulation, while simultaneously mitigating stereotypes associated with aging and the end of the sports career.

Participants will receive instructions and recommendations to facilitate a positive and healthy transition following retirement from elite sport. This minimally active intervention focuses on general guidelines for maintaining an active lifestyle and adapting to post-sport life, ensuring that the control group receives basic informational support without the structured psychoeducational sessions of the experimental group, which allows for an adequate comparison of effects.

Sponsors

University of Salamanca
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

The work of sequencing, randomisation, recruitment and allocation of the trial sample will be carried out by research staff who are not involved in the assessments or interventions of each group, thus avoiding any potential bias in the trial. Participants will also be blinded and will not know which group they have been allocated to and therefore which intervention they will receive. In order to minimise any contamination between groups, the assessment process will be carried out by external research staff who will perform the measurements and who have been previously trained and educated to avoid subjective bias in the process, as they will be unaware of the intervention group to which they have been assigned, thus masking the blinded assessment by third parties in the clinical trial. In addition, the researchers responsible for the statistical analysis of the trial will be blinded in order to increase the rigour of the trial process and thus the scientific quality.

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Participants will be included if they are within the critical transition period, defined as: Five years prior to sports retirement, when the first signs of preparation and emotional anticipation begin. Five years after retirement, the stage in which identity, psychological, and professional adaptation processes are consolidated. This interval reflects the progressive nature of adaptation to sports retirement.

Exclusion criteria

* Athletes presenting any of the following conditions will be excluded from the study: Significant literacy difficulties or relevant deficits in linguistic comprehension that prevent adequate participation in the psychoeducational sessions or the completion of assessment instruments. Severe unstabilized medical or psychological conditions that may interfere with the normal development of the program (e.g., untreated severe depressive episodes, limiting neurological disorders). Failure to meet the inclusion criteria, specifically not being within the five-year period prior to or after sports retirement or failing to verify high-performance sports experience. Refusal to sign the informed consent or lack of availability to regularly attend the program sessions.

Design outcomes

Primary

MeasureTime frameDescription
World Health Organization Quality of Life Measure - Brief Version (WHOQOL-BREF)Baseline; up to 24 weeks; 3 months follow upQuality of life. The range of scores is from 26 to 100 points. The higher the score, the better the quality of life.

Secondary

MeasureTime frameDescription
Satisfaction With Life Scale (SWLS)Baseline; up to 24 weeks; 3 months follow upSatisfaction with life. The range of scores is from 5 to 25 points. A higher score indicates that the person is generally satisfied with his/her life.
Questionnaire of Stereotypes towards Old Age (CENVE)Baseline; up to 24 weeks; 3 months follow upStereotypes about ageing. The range of score is from 5 to 20 points. High scores indicate a high degree of belief in negative stereotypes of ageing.
The acceptance and action questionnaire-II (AAQ-II)Baseline; up to 24 weeks; 3 months follow upPsychological inflexibility. The range of score is from 7 to 49 points. High scores indicate more psychological inflexibility.
MOS Questionnaire of Perceived Social Support (MOS)Baseline; up to 24 weeks; 3 months follow upPerceived social support. The overall scores range from 20 to 100 points. The higher the score, the more social support the individual perceives.
Goldberg General Health Questionnaire (GHQ)Baseline; up to 24 weeks; 3 months follow upPerceived general health. The overall scores range from 0 to 36 points. Higher scores correspond to a higher level of perceived health.
Retirement Attitudes Scale (EAJ)Baseline; up to 24 weeks; 3 months follow upAttitudes towards retirement. The range of scores is from 20 to 140 points. The final scores indicate more negative attitudes the higher the value obtained
Self-Regulation Scale (EAR)Baseline; up to 24 weeks; 3 months follow upSelf-regulation. Scores range from 7 to 35 points. Higher scores on the scale indicate a greater ability to control attention in the pursuit of goals, while lower scores may suggest difficulties in maintaining focus and attention to goals.
Athlete Retirement Questionnaire (ARQ)Baseline; up to 24 weeks; 3 months follow upThis measure will allow assessing the degree of planning, retirement expectations, and knowledge of available resources-all predictive factors of a more satisfactory emotional and functional adjustment (Alfermann et al., 2004). This test consists of 35 items divided into three variables: reasons for retirement (11 items), difficulties encountered during retirement (11 items), and coping strategies (13 items). The questionnaire was translated into Spanish and adapted for active athletes. It shows a Cronbach's alpha of 0.87 for the ARQ retired athletes version and 0.84 for the ARQ active athletes version. The questionnaire consists of 37 and 31 items in each of its versions respectively, with closed-ended responses.
Positive and Negative Affect Schedule (PANAS)Baseline; up to 24 weeks; 3 months follow upIt consists of 10 items each. Participants must indicate how much they have felt each affect on a five-point Likert scale (from 1 = not at all or very slightly to 5 = extremely) during the specified time period. The total for each scale is the summation of the scores given on the 10 items that comprise it, ranging from 10 to 50 points, where a higher score indicates a greater presence of the specific affect. The Spanish version reports high internal consistency, with a Cronbach's α of 0.87 for positive affect and 0.88 for negative affect (Vázquez et al., 2015).
Hospital Anxiety and Depression Scale (HADS)Baseline; up to 24 weeks; 3 months follow upIt was designed to detect anxiety and depression disorders in non-psychiatric hospital settings in patients whose symptoms were not contaminated by the symptomatology of a physical illness. It consists of 14 items grouped into two subscales with 7 items each, using a Likert-type response scale ranging from 0 to 3 points. The depression subscale is composed of items focused on anhedonia. The anxiety subscale is composed of items focused on psychic manifestations. The temporal reference for the test is the previous week. For scoring, separate scores are obtained for each of the subscales, using the following cut-off points: 0-7: normal; 8-10: probable case of anxiety or depression; 11-21: case of anxiety or depression. It possesses a Cronbach's α of 0.90 for the full scale, 0.84 for the depression subscale, and 0.85 for the anxiety subscale.
Generalised Self-Efficacy Scale (EAG)Baseline; up to 24 weeks; 3 months follow upSelf-efficacy. Scores range from 10 to 40 points. Higher scores indicate higher levels of self-efficacy.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026