PACE: The Effect of Solving Jigsaw Puzzles on Visuospatial Cognition in Older Adults: Jigsaw Puzzles As Cognitive Enrichment

Sponsor
University of Ulm (Other)
Overall Status
Completed
CT.gov ID
NCT02667314
Collaborator
Ravensburger Spieleverlag GmbH (RSV), Germany (Other)
100
1
2
24
4.2

Study Details

Study Description

Brief Summary

Meta-analyses indicate beneficial effects of cognitive training and cognitively challenging video games on cognition. However, cognitive effects of solving jigsaw puzzles - a popular, visuospatial cognitive leisure activity - have not been investigated, yet. Thus, the primary aim of this study is to evaluate the effect of solving jigsaw puzzles on visuospatial cognition. As secondary aims, effects on psychological outcomes (self-efficacy, perceived stress, well-being) and visuospatial everyday functioning (instrumental activities of daily living and self-reported cognitive failures in everyday life) are examined.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Jigsaw puzzles
  • Behavioral: Cognitive health counseling
N/A

Detailed Description

see References section below for the study protocol article

Study Design

Study Type:
Interventional
Actual Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Prevention
Official Title:
Jigsaw Puzzles As Cognitive Enrichment
Study Start Date :
Feb 1, 2016
Actual Primary Completion Date :
Feb 1, 2018
Actual Study Completion Date :
Feb 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Jigsaw Puzzle Group

Jigsaw puzzles & Cognitive health counseling

Behavioral: Jigsaw puzzles
Intervention period 1: Participants are asked to solve jigsaw puzzles at home 6 times per week for at least 1 hour over a period of 5 weeks. Intervention period 2 (voluntary): Participants receive the possibility to solve jigsaw puzzles free-of-charge at home for a period of at least 3 month before the 1.5-year follow-up.

Behavioral: Cognitive health counseling
Cognitive health counseling regarding modifiable risk and protective factors of cognitive decline and dementia at baseline, and four telephone calls for expert monitoring (three calls during the 5-week period between pre- and posttest, and one call 12 month later)

Active Comparator: Cognitive Health Counseling Group

Cognitive health counseling only

Behavioral: Cognitive health counseling
Cognitive health counseling regarding modifiable risk and protective factors of cognitive decline and dementia at baseline, and four telephone calls for expert monitoring (three calls during the 5-week period between pre- and posttest, and one call 12 month later)

Outcome Measures

Primary Outcome Measures

  1. Change in global visuospatial cognition from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Averaged score of eight z-standardized visuospatial cognitive ability scores (see secondary outcomes 2 - 9)

Secondary Outcome Measures

  1. Change in visual perception from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Judgment of Line Orientation Test

  2. Change in visuoconstruction from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Copying in Complex Figure Tests; parallel versions for baseline and post-test

  3. Change in mental rotation from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Mental Rotations Test-Letters (2D) and Form A (3D)

  4. Change in visuospatial processing speed from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Trail Making Test A

  5. Change in visuospatial flexibility from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Trail Making Test B

  6. Change in visuospatial working memory from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Block span (Wechsler Memory Scale, German version)

  7. Change in visuospatial reasoning from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Block design (Wechsler Adult Intelligence Scale-III, German version)

  8. Change in visuospatial episodic memory from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Recall in Complex Figure Tests (sum score of immediate and delayed recall); parallel versions for baseline and post-test

  9. Change in psychological health from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Averaged score of three z-standardized psychological health sub-scores (see secondary outcomes 11 - 13)

  10. Change in psychological well-being from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    WHO-Five Well-being Index (WHO-5), German version

  11. Change in self-efficacy from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    General Self-Efficacy Scale, German version

  12. Change in perceived stress from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    Perceived Stress Scale-14, German translation

  13. Change in objective everyday functioning from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    TIADL (1-3): Timed instrumental activities of daily living (Task 1-3; sum-score)

  14. Change in self-reported everyday functioning from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    CFQ (visuospatial items): Cognitive Failures Questionnaire, sum score of visuo-spatial items; German version

  15. Change in jigsaw puzzle performance from baseline to post intervention and to the 1.5-year follow-up [Baseline and post intervention (after 5 weeks and 1.5 years)]

    40-pieces mini puzzle (completed pieces per minute)

  16. Hair cortisol concentration at the 1.5-year follow-up [1.5-year follow-up]

    Hair cortisol will be measured in 1cm segements

  17. Hair dehydroepiandrosteron concentration at the 1.5-year follow-up [1.5-year follow-up]

    Hair dehydroepiandrosteron will be measured in 1cm segements

  18. Hair brain-derived neurotrophic factor concentration at the 1.5-year follow-up [1.5-year follow-up]

    Hair brain-derived neurotrophic factor will be measured in 1cm segements

  19. Neurocognitive disorder [1.5-year follow-up]

    Neurocognitive disorder is a categorical outcome and includes mild and major neurocognitive disorders. Mild neurocognitive disorder (mild cognitive impairment) is defined by subjective cognitive decline (self-report), and an objective cognitive impairments in at least one cognitive abilitiy score (below -1 SD of the norm group), without an essential impairment of daily functioning compared to the premorbid level (self-report). In major neurocognitive decline (dementia), in addition to cognitive decline and impairment, daily functioning is essentially impaired compared to the permorbid level (self-report).

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • No cognitive impairment (Mini-Mental State Examination ≥ 24)

  • Commitment to minimum jigsaw puzzle time (1 hour/day, 6 days/week, 5 weeks)

  • Interest in jigsaw puzzles

  • Low jigsaw puzzle experience (less than 5 completed puzzles within the last 5 years)

Exclusion Criteria:
  • Cognitive impairment (Mini-Mental State Examination < 24)

  • Participation in another interventional study

  • Self-reported psychiatric, neurologic or other disease, which could affect cognitive change over time

  • Self-reported, severe visual impairment or motoric impairment of the upper extremity which significantly affects ability to solve jigsaw puzzles

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinical and Biological Psychology, University of Ulm Ulm Germany

Sponsors and Collaborators

  • University of Ulm
  • Ravensburger Spieleverlag GmbH (RSV), Germany

Investigators

  • Principal Investigator: Iris-Tatjana Kolassa, Prof., University of Ulm, Germany

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Iris Kolassa, Prof. Dr., University of Ulm
ClinicalTrials.gov Identifier:
NCT02667314
Other Study ID Numbers:
  • Klipsy_044_PACE
First Posted:
Jan 28, 2016
Last Update Posted:
Nov 30, 2018
Last Verified:
Nov 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by Iris Kolassa, Prof. Dr., University of Ulm
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 30, 2018